Label: KOCOSTAR FACE THERAPY ACNE TREATMENT CRE AM TO PAT CH- salicylic acid liquid
- NDC Code(s): 83888-020-01
- Packager: FIRSTMARKET CO., LTD.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated June 27, 2024
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Water, Cellulose, Niacinamide, Butylene Glycol, 1,2-Hexanediol, PEG-240/HDI Copolymer Bis-Decyltetradeceth-20 Ether, Caprylic/Capric Triglyceride, Hippophae Rhamnoides Oil, Butylene Glycol Dicaprylate/Dicaprate, Sulfur, Sorbeth-30 Tetraisostearate, Dipropylene Glycol, Sorbitan Sesquiisostearate, Acrylates/Beheneth-25 Methacrylate Copolymer, Tocopherol, Potassium Laurate, PPG-8-Ceteth-20, Capryloyl Salicylic Acid, Melaleuca Alternifolia (Tea Tree) Leaf Extract, Phenoxyethanol, Sodium Lauryl Sulfate, Ethylhexylglycerin, Sodium Benzoate
- PURPOSE
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WARNINGS
For external use only.
Do not use on broken skin. large areas of the skin
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.
Stop use and ask a doctor if irritation becomes severe.
Avoid contact with eyes. If contact occurs, flush thoroughly with water. - KEEP OUT OF REACH OF CHILDREN
- Uses
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Directions
clean the skin thoroughly before applying this productshake welcover the entire affected area with a thin layer using sterile cotton swablet it dry completely and leave in place for 8 hours to permit healingto remove, wet the area with warm water and gently roll with fingertips 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 doctorif bothersome dryness or peeling occurs, reduce application to once a day or every other day
- Other Information
- Questions or comments
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
KOCOSTAR FACE THERAPY ACNE TREATMENT CRE AM TO PAT CH
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83888-020 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 0.5 g in 100 mL Inactive Ingredients Ingredient Name Strength 1,2-HEXANEDIOL (UNII: TR046Y3K1G) NIACINAMIDE (UNII: 25X51I8RD4) WATER (UNII: 059QF0KO0R) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83888-020-01 20 mL in 1 TUBE; Type 0: Not a Combination Product 04/01/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 04/01/2024 Labeler - FIRSTMARKET CO., LTD. (688288012) Registrant - FIRSTMARKET CO., LTD. (688288012) Establishment Name Address ID/FEI Business Operations Natuzen Co.,Ltd. 688201272 manufacture(83888-020)