Label: ACNE TREATMENT MEIJER- salicylic acid gel
- NDC Code(s): 41250-560-51, 41250-560-52
- Packager: MEIJER DISTRIBUTION, INC.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
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.
Drug Label Information
Updated January 4, 2022
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
- Warnings
- When using this product
- Keep out of reach of children.
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Directions
- Cleanse skin thoroughly before applying product.
- Cover the entire afffected 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.
- Other information
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Inactive ingredients
alcohol denat., ammonium hydroxide, benzalkonium chloride, butylene glycol, C12-15 alkyl lactate, C13-14 isoparaffin, capryloyl glycine, cedrus atlantica bark extract, cetyl lactate, cinnamomum zeylanicum bark extract, cocamidopropyl PG-dimonium chloride phosphate, cyclopentasiloxane, dehydroxanthan gum, ethylparaben, fragrance, glycerin, hamamelis virginiana (witch hazel) extract, hexylene glycol, laureth-7, methylparaben, phenethyl dimethicone, phenoxyethanol, polyacrylamide, polysorbate 20, portulaca oleracea extract, PPG-2 isocetheth-20 acetate, propylparaben, sarcosine, tetrasodium EDTA, water
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ACNE TREATMENT MEIJER
salicylic acid gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:41250-560 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 BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) C12-15 ALKYL LACTATE (UNII: GC844VRD7E) C13-14 ISOPARAFFIN (UNII: E4F12ROE70) CAPRYLOYL GLYCINE (UNII: 8TY5YO42NJ) CEDRUS ATLANTICA BARK (UNII: ITP1Q41UPF) COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4) DEHYDROXANTHAN GUM (UNII: 63ZP7I1BQO) ETHYLPARABEN (UNII: 14255EXE39) DIMETHICONE (UNII: 92RU3N3Y1O) AMMONIA (UNII: 5138Q19F1X) CETYL LACTATE (UNII: A7EVH2RK4O) GLYCERIN (UNII: PDC6A3C0OX) HEXYLENE GLYCOL (UNII: KEH0A3F75J) POLYSORBATE 20 (UNII: 7T1F30V5YH) PROPYLPARABEN (UNII: Z8IX2SC1OH) SARCOSINE (UNII: Z711V88R5F) EDETATE SODIUM (UNII: MP1J8420LU) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) HAMAMELIS VIRGINIANA LEAF (UNII: T07U1161SV) PHENOXYETHANOL (UNII: HIE492ZZ3T) POLYACRYLAMIDE (1500 MW) (UNII: 5D6TC4BRWV) LAURETH-7 (UNII: Z95S6G8201) ALCOHOL (UNII: 3K9958V90M) CINNAMON BARK OIL (UNII: XE54U569EC) METHYLPARABEN (UNII: A2I8C7HI9T) PURSLANE (UNII: M6S840WXG5) PPG-2 ISOCETETH-20 ACETATE (UNII: BI6C7YO419) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:41250-560-52 1 in 1 CARTON 09/23/2013 1 NDC:41250-560-51 22.1 mL in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 09/23/2013 Labeler - MEIJER DISTRIBUTION, INC. (006959555)
