LA ROCHE POSAY LABORATORIE DERMATOLOGIQUE EFFACLAR MEDICATED CLEANSER- salicylic acid gel 
L'Oreal USA Products Inc

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Drug Facts

Active ingredient

Salicylic acid 2%

Purpose

Acne treatment

Use

for the treatment of acne

Warnings

For external use only

When using this product

skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Inactive ingredients

water, sodium laureth sulfate, decyl glucoside, glycerin, sodium chloride, coco-betaine, PEG-150 pentaerythrityl tetrastearate, hexylene glycol, sodium hydroxide, PEG-6 caprylic/capric glycerides, zinc gluconate, tetrasodium EDTA, polyquaternium-47, menthol, capryloyl salicylic acid, citric acid

Questions or comments?

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image of a label
LA ROCHE POSAY LABORATORIE DERMATOLOGIQUE EFFACLAR MEDICATED CLEANSER 
salicylic acid gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-023
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID20 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)  
GLYCERIN (UNII: PDC6A3C0OX)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
COCO-BETAINE (UNII: 03DH2IZ3FY)  
PEG-150 PENTAERYTHRITYL TETRASTEARATE (UNII: 8L4OOQ76AM)  
HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
PEG-6 CAPRYLIC/CAPRIC GLYCERIDES (UNII: GO50W2HWO8)  
ZINC GLUCONATE (UNII: U6WSN5SQ1Z)  
MENTHOL (UNII: L7T10EIP3A)  
CAPRYLOYL SALICYLIC ACID (UNII: 5F7PJF6AA4)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49967-023-01200 mL in 1 TUBE; Type 0: Not a Combination Product08/01/2014
2NDC:49967-023-02100 mL in 1 TUBE; Type 0: Not a Combination Product08/01/2014
3NDC:49967-023-0315 mL in 1 TUBE; Type 0: Not a Combination Product10/01/2022
4NDC:49967-023-043 mL in 1 PACKET; Type 0: Not a Combination Product10/01/2022
5NDC:49967-023-05200 mL in 1 TUBE; Type 0: Not a Combination Product10/01/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00608/01/2014
Labeler - L'Oreal USA Products Inc (002136794)
Establishment
NameAddressID/FEIBusiness Operations
L'Oreal USA, Inc.185931458manufacture(49967-023) , pack(49967-023)

Revised: 12/2023
Document Id: 4f240059-6dd5-422b-8ffa-04c6019f4162
Set id: 8a6e2634-2497-403a-af03-113bf35fe36a
Version: 7
Effective Time: 20231231
 
L'Oreal USA Products Inc