VICHY LABORATOIRES NORMADERM DAILY DEEP CLEANSING- salicylic acid gel

Vichy Laboratoires Normaderm Daily Deep Cleansing by

Drug Labeling and Warnings

Vichy Laboratoires Normaderm Daily Deep Cleansing by is a Otc medication manufactured, distributed, or labeled by L'Oreal USA Products Inc, Cosmetique Active Products. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Salicylic acid 0.5%

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

• use twice daily
• massage the foam onto a damp face and rinse off with clear water
• avoid the skin around the eyes
• in case of contact with eyes, rinse immediately

Inactive ingredients

water, sodium laureth sulfate, PEG-8, coco-betaine, hexylene glycol, sodium chloride, PEG-120 methyl glucose dioleate, CI 19140, CI 42053, glycolic acid, triethanolamine, sodium benzoate, sodium hydroxide, dipotassium glycyrrhizate, caprylyl glycol, caprylyl salicylic acid, citric acid, fragrance

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

VICHY LABORATOIRES NORMADERM DAILY DEEP CLEANSING 
salicylic acid gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49967-005
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	5 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
COCO-BETAINE (UNII: 03DH2IZ3FY)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)
GLYCOLIC ACID (UNII: 0WT12SX38S)
TROLAMINE (UNII: 9O3K93S3TK)
SODIUM BENZOATE (UNII: OJ245FE5EU)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
CAPRYLOYL SALICYLIC ACID (UNII: 5F7PJF6AA4)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49967-005-01	200 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/01/2012

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	02/01/2012

Labeler - L'Oreal USA Products Inc (002136794)

Establishment
Name	Address	ID/FEI	Business Operations
Cosmetique Active Products		282658798	manufacture(49967-005)