Label: INNISFREE GENTLE RETINOL SALICYLIC ACNE SERUM- salicylic acid gel gel
- NDC Code(s): 71220-088-02
- Packager: Innisfree Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 8, 2025
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENTS
- Purpose
- Uses
- Warnings
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Directions
■ Clean the skin thoroughly before applying this product.
■ Cover the entire affected area with a thin layer one to three times daily.
■ If bothersome dryness or peeling occurs, reduce application to once a day
or every other day.
■ Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed as directed by a doctor. - Other information
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Inactive ingredients
WATER / AQUA / EAU, GLYCERIN, BUTYLENE GLYCOL, NIACINAMIDE, DICAPRYLYL CARBONATE, TROMETHAMINE, BETAINE,
1,2-HEXANEDIOL, HYDROGENATED LECITHIN, AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER, CAPRYLIC/CAPRIC TRIGLYCERIDE, HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE
COPOLYMER, CHOLESTEROL, HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL, ALLANTOIN, LACTOBACILLUS FERMENT LYSATE, GLYCINE SOJA (SOYBEAN) OIL, TOCOPHEROL, TOCOPHERYL ACETATE, SODIUM
METHYL STEAROYL TAURATE, PROPANEDIOL, DAUCUS CAROTA SATIVA (CARROT) ROOT EXTRACT, ETHYLHEXYLGLYCERIN, ADENOSINE, SORBITAN ISOSTEARATE, CAMELLIA SINENSIS SEED EXTRACT, ASIATICOSIDE, MADECASSIC ACID, RETINOL, ASIATIC ACID, PHYTOSPHINGOSINE, STEARYL GLYCYRRHETINATE, HYALURONIC ACID, CERAMIDE NP, BETA-GLUCAN, BETA-CAROTENE - Questions?
- Innisfree GENTLE RETINOL SALICYLIC ACNE SERUM
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INGREDIENTS AND APPEARANCE
INNISFREE GENTLE RETINOL SALICYLIC ACNE SERUM
salicylic acid gel gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71220-088 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 1 g in 50 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) .ALPHA.-TOCOPHEROL, DL- (UNII: 7QWA1RIO01) SODIUM METHYL STEAROYL TAURATE (UNII: JFM219LJ55) SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4) ADENOSINE (UNII: K72T3FS567) ODETIGLUCAN (UNII: Q6X9CNN54X) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) DICAPRYLYL CARBONATE (UNII: 609A3V1SUA) TROMETHAMINE (UNII: 023C2WHX2V) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) ALLANTOIN (UNII: 344S277G0Z) HYALURONIC ACID (UNII: S270N0TRQY) GLYCERIN (UNII: PDC6A3C0OX) NIACINAMIDE (UNII: 25X51I8RD4) BETAINE (UNII: 3SCV180C9W) CHOLESTEROL (UNII: 97C5T2UQ7J) HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL (UNII: 3W1JG795YI) SOYBEAN OIL (UNII: 241ATL177A) PROPANEDIOL (UNII: 5965N8W85T) MADECASSIC ACID (UNII: M7O1N24J82) ASIATIC ACID (UNII: 9PA5A687X5) STEARYL GLYCYRRHETINATE (UNII: 3YYE6VJS0P) BETA CAROTENE (UNII: 01YAE03M7J) CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U) RETINOL (UNII: G2SH0XKK91) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) CAMELLIA SINENSIS SEED (UNII: MRL49Z8AC4) ASIATICOSIDE (UNII: PKO39VY215) CARROT (UNII: L56Z1JK48B) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) CERAMIDE NP (UNII: 4370DF050B) HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4) PHYTOSPHINGOSINE (UNII: GIN46U9Q2Q) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71220-088-02 1 in 1 BOX 03/01/2025 1 30 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 Drug M006 03/01/2025 Labeler - Innisfree Corporation (557822425)
