NDC 81851-205 Skinbutak Chomchom Magicshampoo
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What is NDC 81851-205?
What are the uses for Skinbutak Chomchom Magicshampoo?
Which are Skinbutak Chomchom Magicshampoo UNII Codes?
The UNII codes for the active ingredients in this product are:
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
- ALLANTOIN (UNII: 344S277G0Z)
- ALLANTOIN (UNII: 344S277G0Z) (Active Moiety)
Which are Skinbutak Chomchom Magicshampoo Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- 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)
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".