Label: DR.G A CLEAR ACNE SPOT TREATMENT SERUM- salicylic acid liquid
- NDC Code(s): 51621-412-01
- Packager: GOWOONSESANG COSMETICS CO., LTD.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated September 24, 2024
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- Dosage and administration
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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 medication at a time.
- Avoid contact with eyes. If contact occurs, flush thoroughly with water.
Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center right away.
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Inactive ingredients
Water(Aqua/Eau), 2,3-Butanediol, Butylene Glycol, Alcohol Denat., 1,2-Hexanediol, Lactobacillus Ferment, Glycerin, Ammonium Polyacryloyldimeth yl Taurate, Niacinamide, Panthenol, Tromethamine, Dipotassium Glycyrrhizate, Allantoin, Succinic Acid, Polyglyceryl-10 Laurate, Propanediol, Stevia Rebaudiana Leaf/Stem Extract, Disodium EDTA, Dextrin, Theobroma Cacao (Cocoa) Extract, Centella Asiatica Extract, Houttuynia Cordata Extract, Mentha Aquatica Extract, Mentha Rotundifolia Leaf Extract, Mentha Viridis (Spearmint) Extract, Asiatic Acid, Asiaticoside, Madecassic Acid, Madecassoside, Salix Alba (Willow) Bark Extract
- Use
- Keep out of reach of children.
- Purpose
- Dr.G A CLEAR ACNE SPOT TREATMENT SERUM 45ml
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INGREDIENTS AND APPEARANCE
DR.G A CLEAR ACNE SPOT TREATMENT SERUM
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:51621-412 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 WATER (UNII: 059QF0KO0R) 2,3-BUTANEDIOL (UNII: 45427ZB5IJ) Product Characteristics Color brown Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51621-412-01 1 in 1 BOX 12/01/2024 1 45 mL in 1 BOTTLE, PLASTIC; 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 12/01/2024 Labeler - GOWOONSESANG COSMETICS CO., LTD. (631170768)