VICHY LABORATOIRES NORMADERM PHYTOACTION ACNE CONTROL DAILY MOISTURIZER- 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

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

• clean the skin thoroughly before applying this product
• cover the entire affected area with a thin layer one to three times daily
• because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor
• if bothersome dryness or peeling occurs, reduce application to once a day or every other day

Inactive ingredients

water, glycerin, isononyl isononanoate, butylene glycol, kaolin, zinc sulfate, bifida ferment lysate, sodium hydroxide, sodium polyacrylate, sodium hyaluronate, sodium benzoate, phenoxyethanol, ascorbyl glucoside, hydrolyzed algin, trisodium ethylenediamine disuccinate, biosaccharide gum-1, acrylates/c10-30 alkyl acrylate crosspolymer, fragrance

Questions or comments?

Call toll free 1-877-378-4245

Monday - Friday (9 a.m. to 5 p.m. EST)

image of a label

image of a label
VICHY LABORATOIRES NORMADERM PHYTOACTION ACNE CONTROL DAILY MOISTURIZER 
salicylic acid gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-606
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)  
GLYCERIN (UNII: PDC6A3C0OX)  
ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
KAOLIN (UNII: 24H4NWX5CO)  
ZINC SULFATE (UNII: 89DS0H96TB)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
ASCORBYL GLUCOSIDE (UNII: 2V52R0NHXW)  
TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)  
BIOSACCHARIDE GUM-1 (UNII: BB4PU4V09H)  
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49967-606-011 in 1 CARTON09/01/2020
150 mL in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:49967-606-021 in 1 CARTON09/01/202006/01/2023
23 mL in 1 TUBE; Type 0: Not a Combination Product
3NDC:49967-606-031.5 mL in 1 PACKET; Type 0: Not a Combination Product09/01/202006/01/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00609/01/2020
Labeler - L'Oreal USA Products Inc (002136794)
Establishment
NameAddressID/FEIBusiness Operations
COSMETIQUE ACTIVE PRODUCTION282658798manufacture(49967-606) , pack(49967-606)

Revised: 12/2023
Document Id: e1476124-7048-4d72-a739-927a5ca14316
Set id: b7d0d094-6a5b-4776-9f13-1f8d30542476
Version: 4
Effective Time: 20231211
 
L'Oreal USA Products Inc