Drug Facts

Drug Labeling and Warnings

Drug Details [pdf]

VICHY NORMADERM PORE UNCLOGGING DAILY SCRUB- salicylic acid gel 
Laboratoires Industriels de Vichy (LIDV)

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Drug Facts

Active ingredient

Salicylic acid 0.5%

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 mediation at a time.

Keep out of reach of children.

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

Directions

• use once daily or 2 to 3 times a week
• massage onto a damp face and rinse off with clear water
• in case of contact with eyes, rinse immediately
  

Purpose

    Acne treatment

Inactive ingredients

water, sodium laureth sulfate, glycerin, decyl glucoside, polyethylene, acrylates/C10-30 alkyl acrylate crosspolymer, glycolic acid, green 3, sodium hydroxide, yellow 5, chondrus crispus (carrageenan), jojoba esters, dipotassium glycyrrihizate, chromium hydroxide green, tetrasodium EDTA, caprylyl glycol, capryloyl salicylic acid, fragrance

VICHY NORMADERM PORE UNCLOGGING DAILY SCRUB 
salicylic acid gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66382-003
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)
GLYCERIN (UNII: PDC6A3C0OX)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
GLYCOLIC ACID (UNII: 0WT12SX38S)
FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
CHONDRUS CRISPUS CARRAGEENAN (UNII: UE856F2T78)
DECYL JOJOBATE (UNII: ZL61O8TFZU)
GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
CHROMIUM HYDROXIDE GREEN (UNII: RV8FT8XF5R)
EDETATE SODIUM (UNII: MP1J8420LU)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
CAPRYLOYL SALICYLIC ACID (UNII: 5F7PJF6AA4)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66382-003-01	125 mL in 1 TUBE; Type 0: Not a Combination Product	02/01/2012	06/01/2015

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	02/01/2012	06/01/2015

Labeler - Laboratoires Industriels de Vichy (LIDV) (282658798)

Revised: 8/2019

Document Id: d2488349-6265-4ffb-853c-77202e77b150

34390-5

Set id: 1ac11d03-a53f-40b0-b7f5-87bf5ddd1da3

Version: 4

Effective Time: 20190827