VICHY LABORATOIRES NORMADERM ACNE CONTROL DAILY MOISTURIZER- salicylic acid gel

Vichy Laboratoires Normaderm Acne Control Daily Moisturizer by

Drug Labeling and Warnings

Vichy Laboratoires Normaderm Acne Control Daily Moisturizer by is a Otc medication manufactured, distributed, or labeled by L'Oreal USA Products Inc, COSMETIQUE ACTIVE PRODUCTION. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Salicylic acid...2%

Purpose

Acne treatment

Uses

• for the treatment of acne
• clears acne blemishes and allows skin to heal
• helps prevent new acne blemishes

Warnings

For external use only

Flammable until dry.

Keep away from flames and heat.

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, butylene glycol, isononyl isononanoate, kaolin, hydrolyzed algin, zinc sulfate, bifida ferment lysate, sarcosine, sodium hyaluronate, sodium hydroxide, trisodium ethylenediamine disuccinate, ascorbyl glucoside, acetic acid, acrylates/c10-30 alkyl acrylate crosspolymer, biosaccharide gum-1, caprylyl glycol, lactic acid, maltodextrin, pentylene glycol, sodium polyacrylate, xanthan gum, sodium benzoate, fragrance

Questions or comments?

Call toll free 1-877-378-4249

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

VICHY LABORATOIRES NORMADERM ACNE CONTROL DAILY MOISTURIZER 
salicylic acid gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49967-660
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)
GLYCERIN (UNII: PDC6A3C0OX)
ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
KAOLIN (UNII: 24H4NWX5CO)
ZINC SULFATE (UNII: 89DS0H96TB)
SARCOSINE (UNII: Z711V88R5F)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)
ASCORBYL GLUCOSIDE (UNII: 2V52R0NHXW)
ACETIC ACID (UNII: Q40Q9N063P)
BIOSACCHARIDE GUM-1 (UNII: BB4PU4V09H)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
LACTIC ACID (UNII: 33X04XA5AT)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
PENTYLENE GLYCOL (UNII: 50C1307PZG)
SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J)
XANTHAN GUM (UNII: TTV12P4NEE)
SODIUM BENZOATE (UNII: OJ245FE5EU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49967-660-01	1 in 1 CARTON	06/01/2023
1		50 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M006	06/01/2023

Labeler - L'Oreal USA Products Inc (002136794)

Establishment
Name	Address	ID/FEI	Business Operations
COSMETIQUE ACTIVE PRODUCTION		282658798	manufacture(49967-660) , pack(49967-660)