Garcia v. L'Oreal USA, Inc.

2025 NY Slip Op 34758(U)
New York Supreme Court, New York County·Decided December 9, 2025·No. Index No. 159463/2025·Unpublished·Mary V. Rosado

Opinion

Garcia v L'Oreal USA, Inc.

2025 NY Slip Op 34758(U)

December 9, 2025

Supreme Court, New York County Docket Number: Index No. 159463/2025 Judge: Mary V. Rosado

Cases posted with a "30000" identifier, i.e., 2013 NY Slip Op 30001(U), are republished from various New York State and local government sources, including the New York State Unified Court System's eCourts Service. This opinion is uncorrected and not selected for official publication.

[FILED: NEW YORK COUNTY CLERK 12/10/2025 11:21 AM] INDEX NO. 159463/2025 NYSCEF DOC. NO. 94 RECEIVED NYSCEF: 12/09/2025

SUPREME COURT OF THE STATE OF NEW YORK NEW YORK COUNTY

PRESENT: HON. MARY V. ROSADO PART 33M

, _______________________________ ------X Justice

INDEX NO. 159463/2025 MAYRA GARCIA,

MOTION DATE 09/18/2025 Plaintiff,

MOTION SEQ. NO. -----=-00::....:7_ __ - V -

L'OREAL USA, INC.,L'OREAL USA PRODUCTS, INC.,SOFT SHEEN-CARSON, LLC,STRENGTH OF DECISION + ORDER ON

NATURE, LLC,GODREJ SON HOLDINGS, INC.,LUSTER PRODUCTS COMPANY, NAMASTE LABORATORIES, LLC MOTION

Defendant.

----------------------------X

The following e-filed documents, listed by NYSCEF document number (Motion 007) 35, 36, 37, 38, 39, 63, 64, 65, 66, 67, 68, 69, 70, 71, 79, 80, 81 were read on this motion to/for DISMISS

Upon the foregoing documents, and after a final submission date of November 5, 2025, Defendants L'Oreal USA, Inc., L'Oreal USA Products, Inc., and SoftSheen-Carson LLC's (collectively, "L'Oreal USA") motion to dismiss Plaintiff Mayra Garcia's ("Plaintiff'') Complaint is denied.

I. Background

This action arises out of Plaintiff's alleged exposure to hair straightening products which allegedly caused endometrial cancer. From the 1970s through 2006, Plaintiff alleges she used numerous hair relaxer products manufactured and sold by Defendants. In or around September of 2022, Plaintiff was diagnosed with endometrial adenocarcinoma, and in March of2023 underwent surgery for an incarcerated hernia allegedly due to complications from her cancer treatment. Plaintiff now sues Defendants under numerous theories of liability seeking to recover damages related to her uterine cancer diagnosis. L'Oreal responds with the instant pre-answer motion to

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dismiss. Plaintiff opposes and requests leave to amend or supplement her Complaint should the Court find her Complaint deficient in any regard. 1 II. Discussion

A. Preemption

L'Oreal's motion to dismiss based on express preemption is denied. Defendants argue Plaintiffs claims are expressly preempted by the Food, Drug, and Cosmetic Act ("FDCA"), 21 U.S.C. §301. Express preemption applies only where the plain language of a statute supersedes state law (Doomes v Best Transit Corp., 17 NY3d 594, 601 [2011 ]). As held by the United States Supreme Court, there is a presumption against pre-emption, and pre-emption clauses are to be narrowly construed (Cipollone v Liggett Group, Inc. 505 U.S. 504, 505 [1992]; see also Galper v JP Morgan Chase Bank, NA., 802 F3d 437, 448 [2d Cir 2015]). The specific language which L'Oreal argues preempts many of Plaintiffs causes of action is found in 21 U.S.C. § 379s(a).

That provision provides:

"Except as provided in subsection (b), (d), or (e), no State or political subdivision of a State may establish or continue in effect any requirement for labeling or packaging of a cosmetic that is different from or in addition to, or that is otherwise not identical with, a requirement specifically applicable to a particular cosmetic or class of cosmetics under this chapter, the Poison Prevention Packaging Act of 1970 (15 U.S.C. 1471 et seq.), or the Fair Packaging and Labeling Act (15 U.S.C. 1451 et seq.)."

The exception to the preemption clause found at 21 U.S.C. § 379s(d) provides:

"Nothing in this section shall be construed to modify or otherwise affect any action or the liability of any person under the product liability law of any State."

A holistic review of Plaintiffs Complaint yields allegations that Defendants were negligent for failure to comply with the labelling requirements of 21 U.S.C. §§ 361,362, and 21 C.F.R. §

1 Plaintiff did not fonnally cross-move for a motion to amend, therefore the Court need not entertain this relief (see

Fifth Partners LLC v Foley, 227 AD3d 543 [1st Dept 2024]; Onofre v 243 Riverside Drive Corp., 232 AD3d 443, 443-444 [1st Dept 2024]).

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740.1 (a). Accepting Plaintiff's allegations as true, pursuant to § 361, titled "Adulterated cosmetics," Defendants' products should have been labelled and/or recalled as adulterated. That section specifically states a cosmetic is adulterated "[i]f it bears or contains any poisonous or deleterious substance which may render it injurious to users under the conditions of use prescribed in the labelling thereof, or under such conditions of use as are customary or usual.. .. " (see 21 U.S.C. § 361[a]). Moreover, pursuant to 21 U.S.C. 362(a), a cosmetic is misbranded "[i]f its labelling is false or misleading in any particular (sic)." And pursuant to 21 C.F.R. § 740. l(a), "[t]he label of a cosmetic product shall bear a warning statement whenever necessary or appropriate to prevent a health hazard that may be associated with the product."

L'Oreal's preemption argument is misguided in two respects. First, Plaintiff does not seek relief under state law causes of action that would impose a different or additional labeling requirement pursuant to the FDCA. Rather, Plaintiff is alleging state law causes of action based on purported violations of the FDCA's labeling requirement. Specifically, it is alleged that Defendants' products were marketed and sold as "safe" and "natural" even though there was scientific data showing certain ingredients in Defendants' products disrupt women's endocrine systems (NYSCEF Doc. 1 at ,i,i 81-82). These ingredients are alleged to include, but are not limited to, phthalates, parabens, cyclosiloxanes, di-(2-ethlhexyl), octamethylcyclotetrasiloxane, lye, and formaldehyde (Id. at ,i,i 43-62). Given the presumption against preemption and construing 21 U.S.C. § 379s(a) narrowly and in conjunction with other sections of the FDCA, the Court finds Plaintiff's sixth through tenth causes of action and twelfth cause of action are not expressly preempted. Indeed, § 379s(a) does not expressly bar plaintiffs from using common law causes of action to seek damages based on a defendant's alleged failure to comply with the labeling requirements set forth in the FDCA.

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