Trademark Trial and Appeal Board Electronic Filing System. http://estta.uspto.gov
`
`ESTTA Tracking number:
`
`ESTTA1088088
`
`Filing date:
`
`10/12/2020
`
`IN THE UNITED STATES PATENT AND TRADEMARK OFFICE
`BEFORE THE TRADEMARK TRIAL AND APPEAL BOARD
`
`Proceeding
`
`92067467
`
`Party
`
`Correspondence
`Address
`
`Plaintiff
`New Enchantment, LLC
`
`MICHAEL A GROW
`ARENT FOX LLP
`1717 K STREET NW
`WASHINGTON, DC 20006
`UNITED STATES
`Primary Email: tmdocket@arentfox.com
`Secondary Email(s): michael.grow@arentfox.com,
`chiara.giuliani@arentfox.com, danielle.bulger@arentfox.com,
`teresa.myers@arentfox.com
`202-857-6000
`
`Submission
`
`Filer's Name
`
`Filer's email
`
`Signature
`
`Date
`
`Attachments
`
`Plaintiff's Notice of Reliance
`
`Michael A. Grow
`
`michael.grow@arentfox.com
`
`/Michael A. Grow/
`
`10/12/2020
`
`Notice of Reliance - Official Records and Printed Publications and Ex hibits D-
`M.pdf(296902 bytes )
`Exhibit D.pdf(78222 bytes )
`Exhibit E.pdf(840480 bytes )
`Exhibit F pt 1.pdf(4380928 bytes )
`Exhibit F pt 2.pdf(3809924 bytes )
`Exhibit F pt 3.pdf(5743315 bytes )
`Exhibit F pt 4.pdf(4094038 bytes )
`Exhibit G.pdf(5564197 bytes )
`Exhibit H pt 1.pdf(3304823 bytes )
`Exhibit H pt 2.pdf(4846414 bytes )
`
`

`

`
`
`IN THE UNITED STATES PATENT AND TRADEMARK OFFICE
`
`BEFORE THE TRADEMARK TRIAL AND APPEAL BOARD
`
`
`____________________________________
`
`
`
`
`
`
`)
`NEW ENCHANTMENT, LLC
`
`)
`)
`)
`
`Petitioner,
`
`
`
`
`
`
`
`
`
`
`Reg. Nos. 85084121 and 5790684
`
`
`Mark: MIAMO &
`
`
`
`Consolidated Cancellation No. 92067467
`
`
`
`
`
`v.
`
`
`
`
`
`
`
`
`
`)
`)
`)
`
`
`
`MEDSPA S.R.L.
`)
`
`
`
`
`
`
`)
`
`
`
`
`Registrant.
`____________________________________)
`
`
`PETITIONER’S NOTICE OF RELIANCE
`ON OFFICIAL RECORDS AND PRINTED PUBLICATIONS
`
`
`Pursuant to Rule 2.122(e) of the Trademark Rules of Practice, New Enchantment,
`
`
`
`LLC (“Petitioner”), hereby gives notice that it will rely upon the following printed publications,
`
`such as website printouts, available to the general public, in libraries, or of general circulation
`
`among members of the public, or that segment of the public which are relevant under the issues
`
`in this proceeding:
`
`
`
`Exhibit D: A true and correct copy of a printout from the Google Translate website, located at
`
`<translate.google.com>. This printout is being offered in evidence to show that “mi amo” is the
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`Italian translation for the English phrase “I love myself.”
`
`
`
`Exhibit E: A true and correct copy of a printout from the official website of the U.S. Food and
`
`Drug Administration (“FDA”), located at <http://www.fda.com>. This printout contains an
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`excerpt from the official Federal Food, Drug & Cosmetic Act (FD&C Act), which defines
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`cosmetics as "articles intended to be rubbed, poured, sprinkled, or sprayed on, introduced into, or
`
`AFDOCS/22972088.1
`
`
`

`

`
`
`otherwise applied to the human body...for cleansing, beautifying, promoting attractiveness, or
`
`altering the appearance." On this same page, the FDA explains that “[i]ncluded in this definition
`
`are products such as skin moisturizers, perfumes, lipsticks, fingernail polishes, eye and facial
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`makeup preparations, shampoos, permanent waves, hair colors, toothpastes, and deodorants, as
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`well as any material intended for use as a component of a cosmetic product.”
`
`
`
`Exhibit F: True and correct copies of printouts from the website located at
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`<www.Miiamo.com> showing products available for purchase and MII AMO goods and
`
`services. These are being offered in evidence to representatively demonstrate Petitioner’s use of
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`the MII AMO Mark, to show similarity and relatedness of the parties’ goods and services and
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`trade channels, and the conditions under which and buyers to whom sales are made.
`
`
`
`Exhibit G: True and correct copies of printouts from the website located at
`
`<www.Miamo.com> showing products available for purchase and MIAMO goods and services.
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`These are being offered in evidence to representatively demonstrate Registrant’s use of the
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`MIAMO Mark, to show similarity and relatedness of the parties’ goods and services and trade
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`channels, and the conditions under which and buyers to whom sales are made.
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`
`
`Exhibit H: True and correct copies of printouts from www.web.archive.org showing products
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`available for purchase from 2001-2013 on www.Miiamo.com. This is being offered in evidence
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`to show priority of Petitioner’s MII AMO Mark and Petitioner’s use of its MII AMO Mark.
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`
`
`AFDOCS/22972088.1
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`
`

`

`
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`Exhibit I: True and correct copies of documents printed from the U.S. Patent and Trademark
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`Office website for the file relating to U.S. Trademark Application Serial No. 86/257,212,
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`including a Letter of Protest Memorandum, a status page, a Notice of Abandonment, and an
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`Office Action.
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`
`
`Exhibit J: True and correct copies of printouts from the U.S. Patent and Trademark Office
`
`website showing that no one else but MedSpa S.R.L. and Erva Bonita Inc. has applied for or
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`registered MIAMO in Classes 3, 5, 35 or 44.
`
`
`
`Exhibit K: True and correct printouts from the Arizona Corporation Commission related to New
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`Enchantment’s corporate registration.
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`
`
`Exhibit L: True and correct printout from the ICANN WHOIS registration database, located at
`
`<www.whois.networksolutions.com>, regarding the Miiamo.com domain name and website, and
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`showing a creation date of November 23, 1999. This is being offered in evidence to show
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`priority of Petitioner’s MII AMO Mark and Petitioner’s use of its MII AMO Mark.
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`
`
`Exhibit M: True and correct excerpts of printouts from the MII AMO Facebook, Twitter,
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`Pinterest, and Instagram social media pages.
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`
`
`
`
`
`
`
`
`Dated: October 12, 2020
`
`
`
`
`
`
`
`
`
`
`
`Respectfully submitted,
`
`/Michael A. Grow/
`Michael A. Grow
`Danielle W. Bulger
`
`
`
`AFDOCS/22972088.1
`
`
`

`

`
`
`Arent Fox LLP
`1717 K Street, N.W.
`Washington, D.C. 20006
`(202) 857-6000
`
` Attorneys for Petitioner
`New Enchantment, LLC
`
`
`
`AFDOCS/22972088.1
`
`
`

`

`
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`
`
`
`
`CERTIFICATE OF SERVICE
`
`I hereby certify that I served a copy of the foregoing Petitioner’s Notice of Reliance on
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`Official Records and Printed Publications (re: Consolidated Cancellation Proceeding No.
`
`92067467) upon Registrant’s counsel of record Jason Cooper of The Sladkus Law Group,
`
`located at 1397 Carroll Drive, Atlanta, GA 30318, via e-mail (at jeff@sladlaw.com,
`
`jason@sladlaw.com, mandy@sladlaw.com), on this 12th day of October, 2020.
`
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`
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`
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`
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`/Danielle W. Bulger/
`
`
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`
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`AFDOCS/22972088.1
`
`
`

`

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`EXHIBIT D
`EXHIBIT D
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`

`

`2 Google Translate
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`
`
`7A Text
`
`. Documents
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`ITALIANr DETECTED
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`ENGLISH
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`SPANISH
`
`FRENCH
`
`v
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`J’
`
`ENGLISH
`
`SPANISH
`
`ARABIC
`
`mi amo
`
`X
`
`I love myself @
`
`'9: Transa.eIro|n Spanish
`
`
`
`5/5000
`
`‘9
`
`I; /<
`send feedbark
`
`O
`HIstcry
`
`*
`Saved
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`2;
`Communitv
`
`[hups/ltnnslate.google.oom/#view=home&op=tlanslateksl=autoaxtl=en&text mi amo] - [10-09-2020, 16:
`
` 6:41]
`
`

`

`
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`EXHIBIT E
`EXHIBIT E
`
`

`

`
`g An atncra website ottne United statesgovernment Here's new /ou know v
`FDA U.S. FOOD & DRUG
`
`rtnmmmzrnan - Home / Cosmetics / Cosmetics Guidance it Regulation / Cosmetics Laws E Regulations / Cosmetics & U 8 Law
`
`Cosmetics Laws 5 Regulations
`
`Key Leqal Conceots tor
`Cosmetics troustry: interstate
`Commerce, Adul'erated and
`Misb'anded
`
`Regulations Related to
`Cosmetics from Title 21 ofthe
`Code of Federal Regulations
`(Zt CFR)
`Prohibited it Restricted
`Ingredients m Cosmetics
`Cosmetics 11 U.S Law
`
`Cosmetics & U.S. Law
`I Stare
`at tweet
`in rrmemn
`EEmaII 9 Print
`
`Tire following is an introduction to how cosmetics are regulated under U.S. law, and how
`these laws may be different from those in other countries.
`On this page:
`- Introduction
`0 How U.S. law Defines Cosmetics
`0 How U.S. Law Defines Drugs
`0 How a Product Can Be Considered Both :1 Cosmetic
`and a Drug
`0 Assuring Ingredient and Product Safety
`0 Cosmetics Registration
`0 More Resources
`
`Translations
`- French (PDF‘ 88KB)
`Spanish (PDF 891(3)
`Si'l‘l‘lifli’d Chin“? (PDF "31(3)
`Traditional Chinese (PDF 181KB)
`Knrean (PDF‘ 152KB)
`
`Content current as of:
`UBI'ZIUZU'ZO
`Regulated Product[s)
`Cosmetics
`
`Introduction
`Among the important differences between requirements for cosmetics in the United States
`and various other countries are the legal definitions of drugs and cosmetics, restrictions on
`the use of color additives and other ingredients, and registration requirements, Some
`products regulated as cosmetics in Europe, for instance, are regulated as drugs in the
`United States. Sunscreens are a case in point. There also are differences regarding
`prohibited and restricted ingredients, particularly color additives. Some countries may
`require cosmetic companies to register their establishments and list products and
`ingredients with the government; in the United States, cosmetic registration is voluntary
`but highly recommended
`How U.S. Law Defines Cosmetics
`The Federal Food, Drug & Cosmetic Act (FD&C Act) defines cosmetics as "articles
`intended to be rubbed, poured, sprinkled, or sprayed on, introduced into, or otherwise
`applied to the human body...for cleansing, beautifying, promoting attractiveness, or
`altering the appearance." Included in this definition are products such as skin
`moisturizers, perfumes. lipsticks, fingernail polishes. eye and facial makeup preparations,
`shampoos. permanent waves. hair colors. toothpastes, and deodorants, as well as any
`material intended for use as a component ofa cosmetic product.
`
`How U.S. Law Defines Drugs
`Tire FD&C Act defines drugs as "articles intended for use in the diagnosis, cure, mitigation,
`treatment, or prevention of disease...and articles (other than food) intended to affect the
`structure or any function of the body ofman or other animals." Over-the-counter (OTC)
`dmgs are drugs that can be purchased without a doctor's prescription.
`The agency is conducting a review of all OTC drugs to establish monographs (rules) under
`which the drugs are generally recognized as safe and effective, and not misbranded. These
`rules are established on a class-by—class basis (for arample, fluoride dentifrices, cough
`suppressants, and anh'histamines). OTC drugs must meet the requirements ofthe
`appropriate class once that rule is published as a final regulation.
`If an OTC drug does not meet the requirements of the appropriate final rule, it is
`considered a misbranded drug and a "new drug." A "new drug" must have an approved
`New Drug Application (NDA) before it may be introduced into interstate commerce. In
`addition, drug manufacturers must comply with Good Manufacturing Practice regulations.
`Certain claims may cause a product to qualify as a drug, even ifthe product is marketed as
`if it were a cosmetic. Such claims establish the product as a drug because the intended use
`is to treat or prevent disease or otherwise affect the structure or functions ofthe human
`body. Some examples are claims that products will restore hair growth, roducc cellulite,
`treat varicose veins, or revitalize cells.
`
`How a Product Can Be Considered Both a Cosmetic and a Drug
`OTC drugs are often marketed side by side with cosmetics, and some products qualify both
`as cosmetics and as OTC drugs. This mayhappen when a product has two intended uses,
`with ingredients intended to do two different things. For instance, a shampoo is a
`cosmetic, since is intended use is to cleanse the hair. An untiedandrufftreatment is a
`dmg, because its intended use is to treat dandruff. Consequently, an antidandruff
`shampoo is both a cosmetic and a drug. Among other cosmetic/drug combinations are
`toothpastm that contain fluoride, deodorants that are also antiperspirants, and
`moisturizers and makeup marketed willr sun-protection claims.
`
`Assuring Ingredient and Product Safety
`Cosmetics imported into the United States, both ingredients and finished products, must
`meet the same criteria for safety and labeling as those manufactured domestically.
`FDA does not pre-approve cosmetic products or ingredients, with the important exception
`of color additives. However, cosmetic firms are responsible for marketing safe, properly
`labeled products; using no prohibited ingredients; and adhering to limits on restricted
`ingredients. It is also considered good practice to follow industry safety guidelines and
`recommendations.
`
`Before marketing a product containing a color additive in the United States, it is essential
`to determine whether the additive is approved for its intended use. A number ofcolor
`additives must be certified for purity in FDAlabs ifthey are to be used legally in a product
`marketed in the United States.
`
`Although U.S. regulations do not specify any particular testing regimens for cosmetic
`products or ingredients, it is the cosmetic company's responsibilityto subsmntiate product
`and ingredient safety prior to marketing.
`
`Cosmetic Registration
`
`[llttps://www.fda.gov/oosmetics/cosmetiI:-Iaws-reguIations/cosmetics-us-Iaw] - [10-09-2010, 16:26:40]
`
`

`

`Cosmetic companies may register in the United States through FDA's Voluntary Cosmetic
`Registration Program (VCKJ’J, 'lhe VCKP assists FDA in carrying out its responsibility to
`regulate cosmetics. FDA uses the, information to evaluate cosmetic products on the
`market Because product filings and establishment registrations are not mandatory,
`Voluntary submissions provide FDA with the best information available about cosmetic
`products and ingredients, their frequency ofuse, and businesses engaged in their
`manufacture and distribution (Federal Register, vol. 73, p. 76360, and vol. 69, p. 9339).
`More Resources
`FDA Authority Over Cosmetics
`Color Additives Permitted for Use in Cosmetics
`Guidance 8: Regulations
`International Activities
`Is It a Cosmetic, a Drug, or Both? (Or Is It Soap?)
`Key Legal Concepts: Interstate Commerce, Adulterated, and Misbranded
`Labeling
`Products & Ingredients
`Resources for You
`ls It a Cosmetic, a Ding, or Both? (01‘ Is It Soap?)
`International Harmonization; Policy on Standards; Notice--Federal Register, vol. 60
`
`FDA Archive
`About FDA
`
`Accessibility
`
`Visitor Information
`
`website Policies / Privacy
`No FEAR Act
`
`FOIA
`
`HHs.gov
`USA.gov
`
`@lfv-h
`
`L ‘l-BSE-lNFOFDA (1-838-463-6332)
`
`[https://www.fda.gov/oosmetics/cosmetiI:-Iaws-reguIations/cosmetics-us-Iaw] - [10-09-2010, 16:26:40]
`
`

`

`EXHIBIT F, pt. 1
`EXHIBIT F, pt. 1
`
`

`

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`EXHIBIT F, pt. 2
`EXHIBIT F, pt. 2
`
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`Page 2
`Mii amo Face 81 Body Products: Shop Mii amo
`https:lishop.miiamo.com/m -amo-face-body
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