Label: SKINBUTAK CHOMCHOM MAGICSHAMPOO- allantoin, salicylic acid shampoo
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Contains inactivated NDC Code(s)
NDC Code(s): 81851-205-01 - Packager: NatureBlue Co.,Ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not 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 April 29, 2021
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Uses
- Warnings
- Stop use and ask doctor if
- When using this product
- Keep out of reach of children
- Directions
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Inactive Ingredients
Purified water, Polyquaternium-10, Sodium Benzoate, Allantoin, Disodium Laureth Sulfosuccinate, Cocamidopropy1 Betaine,TEA-Cocoy1 Glutamate, Potassium Cocoy1 Glycinate, Cocamide DEA, Menthol, Salicylic Acid, Panthenol, Hydrolyzed Wheat Protein, Sodium Lauroyl Hydrolyzed Silk, Propylene Glycol Laurate, Hippophae Rhamnoides Fruit Oil, Olea Europaca(Olive) Fruit Oil, Morus Alba Root Extract, Camellia Sinensis Leaf Extract, Calendual Officinalis Extract, Swertia Japonica Extract, Aloe Barbadensis Leaf Extract, Sophora Angustifolia Root Extract, Fragrance
- Other Information
- Package Label
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INGREDIENTS AND APPEARANCE
SKINBUTAK CHOMCHOM MAGICSHAMPOO
allantoin, salicylic acid shampooProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81851-205 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 0.25 mg in 100 mL ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) ALLANTOIN 1 mg in 100 mL Inactive Ingredients Ingredient Name Strength DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E) MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) HYDROLYZED WHEAT PROTEIN (ENZYMATIC, 3000 MW) (UNII: J2S07SB0YL) GREEN TEA LEAF (UNII: W2ZU1RY8B0) POTASSIUM COCOYL GLYCINATE (UNII: WZ70FUF22U) PROPYLENE GLYCOL MONOLAURATE (UNII: 668Z5835Z3) HIPPOPHAE RHAMNOIDES FRUIT OIL (UNII: TA4JCF9S1J) OLIVE OIL (UNII: 6UYK2W1W1E) CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) TRIETHANOLAMINE COCOYL GLUTAMATE (UNII: LA19WH54UL) PANTHENOL (UNII: WV9CM0O67Z) MORUS ALBA ROOT (UNII: CST1G9BZGD) SWERTIA JAPONICA WHOLE FLOWERING (UNII: 01X0P6GX6C) ALOE VERA LEAF (UNII: ZY81Z83H0X) WATER (UNII: 059QF0KO0R) SODIUM BENZOATE (UNII: OJ245FE5EU) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K) COCO DIETHANOLAMIDE (UNII: 92005F972D) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:81851-205-01 300 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/03/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 05/03/2021 Labeler - NatureBlue Co.,Ltd (689062549) Registrant - NatureBlue Co.,Ltd (689062549) Establishment Name Address ID/FEI Business Operations NatureBlue Co.,Ltd 689062549 manufacture(81851-205)