CERAVE DEVELOPED WITH DERMATOLOGISTS ACNE CONTROL CLEANSER- salicylic acid gel

Drug Labeling and Warnings

Drug Details [pdf]

Medicinal ingredient (w/w)

Salicylic acid 2%

Warnings

For external use only

Ask a doctor before use

if you have severe acne.

When using this product

skin irritation and dryness are more likely to occur when using another topical acne product at the same time. If irritation occurs, use only one product at a time. Avoid contact with eyes. If contact occurs, rinse thoroughly with water.

Keep out of reach of children.

If swallowed, call a poison control centre or get medical help right away.

Directions

Adults and adolescents 12 years and older. For New Users: Apply product to a small area once a day for three days to test if you are sensitive to this product. If no discomfort occurs, cover the entire affected area with a thin layer. Start with one application daily, then gradually increase to two or three times daily, if needed. If dryness or peeling occurs, reduce application to once a day or every other day. Rinse off.

Questions?

1-888-399-3603

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CERAVE DEVELOPED WITH DERMATOLOGISTS ACNE CONTROL CLEANSER 
salicylic acid gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82046-481
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	20 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618)
COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W)
GLYCERIN (UNII: PDC6A3C0OX)
NIACINAMIDE (UNII: 25X51I8RD4)
GLUCONOLACTONE (UNII: WQ29KQ9POT)
SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493)
SODIUM METHYL COCOYL TAURATE (UNII: JVL98CG53G)
PEG-150 PENTAERYTHRITYL TETRASTEARATE (UNII: 8L4OOQ76AM)
XANTHAN GUM (UNII: TTV12P4NEE)
SODIUM BENZOATE (UNII: OJ245FE5EU)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
HECTORITE (UNII: 08X4KI73EZ)
TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)
SODIUM LAUROYL LACTYLATE (UNII: 7243K85WFO)
CHOLESTEROL (UNII: 97C5T2UQ7J)
COCONUT ACID (UNII: 40U37V505D)
EDETATE SODIUM (UNII: MP1J8420LU)
CALCIUM GLUCONATE (UNII: SQE6VB453K)
CERAMIDE NP (UNII: 4370DF050B)
TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
CERAMIDE AP (UNII: F1X8L2B00J)
PHYTOSPHINGOSINE (UNII: GIN46U9Q2Q)
HYALURONIC ACID (UNII: S270N0TRQY)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
BENZOIC ACID (UNII: 8SKN0B0MIM)
CERAMIDE 1 (UNII: 5THT33P7X7)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82046-481-01	237 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/19/2026
2	NDC: 82046-481-02	355 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/19/2026
3	NDC: 82046-481-03	473 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/19/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Export only		05/19/2026

Labeler - L'Oreal USA Products Inc (002136794)

Establishment
Name	Address	ID/FEI	Business Operations
L'OREAL USA, INC.		960317444	manufacture(82046-481) , pack(82046-481)

Establishment
Name	Address	ID/FEI	Business Operations
L'Oreal USA Products, Inc.		624244349	manufacture(82046-481) , pack(82046-481)

Establishment
Name	Address	ID/FEI	Business Operations
Dimensional Merchandising Inc.		076693183	pack(82046-481)