NDC 69838-001 Haircop Hairdanbi Natural
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 69838-001?
What are the uses for Haircop Hairdanbi Natural?
Which are Haircop Hairdanbi Natural UNII Codes?
The UNII codes for the active ingredients in this product are:
- PANTHENOL (UNII: WV9CM0O67Z)
- PANTHENOL (UNII: WV9CM0O67Z) (Active Moiety)
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Haircop Hairdanbi Natural 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:
- WATER (UNII: 059QF0KO0R)
- AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)
- DISODIUM LAURYL SULFOSUCCINATE (UNII: P160Q81342)
- COCO MONOETHANOLAMIDE (UNII: C80684146D)
- DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)
- SCHISANDRA CHINENSIS FRUIT (UNII: ABS794681C)
- FALLOPIA MULTIFLORA ROOT (UNII: AUZ3VD75MC)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A)
- POLYQUATERNIUM-10 (400 MPA.S AT 2%) (UNII: HB1401PQFS)
- MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- HYALURONIC ACID (UNII: S270N0TRQY)
- HOUTTUYNIA CORDATA FLOWERING TOP (UNII: RH041UUZ22)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- GERANIUM OIL, ALGERIAN TYPE (UNII: 5Q1I94P4WG)
What is the NDC to RxNorm Crosswalk for Haircop Hairdanbi Natural?
- RxCUI: 1650439 - panthenol 0.1 % / salicylic acid 0.1 % Medicated Shampoo
- RxCUI: 1650439 - panthenol 1 MG/ML / salicylic acid 1 MG/ML Medicated Shampoo
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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".