VICHY LABORATOIRES NORMADERM PHYTOACTION DAILY DEEP CLEANSING- salicylic acid gel 
L'Oreal USA Products Inc

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Drug Facts

Active ingredient

Salicylic acid...0.5%

Purpose

Acne treatment

Use

for the treatment of acne

Warnings

For external use only

When using this product

kin 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, coco-betaine, propanediol, PEG-120 methyl glyucose dioleate, sodium chloride, sodium cocoyl glycinate, dipropylene glycol, zinc gluconate, bifida ferment lysate, sodium hydroxide, sodium benzoate, phenoxyethanol, copper gluconate, caprylyl glycol, tetrasodium glutamate diacetate, fragrance

image of a label

image of a label
VICHY LABORATOIRES NORMADERM PHYTOACTION DAILY DEEP CLEANSING 
salicylic acid gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-307
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Salicylic Acid (UNII: O414PZ4LPZ) (Salicylic Acid - UNII:O414PZ4LPZ) Salicylic Acid5 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
COCO-BETAINE (UNII: 03DH2IZ3FY)  
PROPANEDIOL (UNII: 5965N8W85T)  
PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM COCOYL GLYCINATE (UNII: XLU9KH03XM)  
DIPROPYLENE GLYCOL (UNII: E107L85C40)  
ZINC GLUCONATE (UNII: U6WSN5SQ1Z)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
COPPER GLUCONATE (UNII: RV823G6G67)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49967-307-01200 mL in 1 BOTTLE; Type 0: Not a Combination Product04/15/2020
2NDC:49967-307-027 mL in 1 PACKET; Type 0: Not a Combination Product04/29/2020
3NDC:49967-307-0350 mL in 1 BOTTLE; Type 0: Not a Combination Product08/18/202008/18/2020
4NDC:49967-307-0415 mL in 1 BOTTLE; Type 0: Not a Combination Product08/18/202008/18/2020
5NDC:49967-307-05400 mL in 1 BOTTLE; Type 0: Not a Combination Product11/15/2022
6NDC:49967-307-0650 mL in 1 TUBE; Type 0: Not a Combination Product08/18/202006/01/2023
7NDC:49967-307-0715 mL in 1 TUBE; Type 0: Not a Combination Product08/18/202006/01/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00604/15/2020
Labeler - L'Oreal USA Products Inc (002136794)
Establishment
NameAddressID/FEIBusiness Operations
COSMETIQUE ACTIVE PRODUCTION282658798manufacture(49967-307) , pack(49967-307)
Establishment
NameAddressID/FEIBusiness Operations
Socoplan276221405pack(49967-307)

Revised: 12/2023
Document Id: 82bf925d-f4a8-400b-a2f8-68f6e9ba94be
Set id: 0db3a8cb-7691-4772-9f7d-15de66098e2e
Version: 10
Effective Time: 20231211
 
L'Oreal USA Products Inc