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

image of a label

VICHY NORMADERM PORE UNCLOGGING DAILY SCRUB 
salicylic acid gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 66382-003
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)  
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 66382-003-01125 mL in 1 TUBE; Type 0: Not a Combination Product02/01/201206/01/2015
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D02/01/201206/01/2015
Labeler - Laboratoires Industriels de Vichy (LIDV) (282658798)

Revised: 8/2019
 

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