NDC 61995-0129 J1002901jason Dandruff Relief 2in1treatment
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 61995 - The Hain Celestial Group, Inc.
- 61995-0129 - J1002901jason Dandruff Relief 2in1treatment
Product Packages
NDC Code 61995-0129-8
Package Description: 355 g in 1 BOTTLE
Product Details
What is NDC 61995-0129?
What are the uses for J1002901jason Dandruff Relief 2in1treatment?
Which are J1002901jason Dandruff Relief 2in1treatment UNII Codes?
The UNII codes for the active ingredients in this product are:
- PYRITHIONE ZINC (UNII: R953O2RHZ5)
- PYRITHIONE ZINC (UNII: R953O2RHZ5) (Active Moiety)
Which are J1002901jason Dandruff Relief 2in1treatment 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:
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- WATER (UNII: 059QF0KO0R)
- SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493)
- GLYCERIN (UNII: PDC6A3C0OX)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- BABASSU OIL (UNII: 8QSB4M5477)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- JOJOBA OIL (UNII: 724GKU717M)
- ZINC CARBONATE (UNII: EQR32Y7H0M)
- GUAR GUM (UNII: E89I1637KE)
- DIHEPTYL SUCCINATE (UNII: 057N7SS26Y)
- PYRROLIDONE CARBOXYLIC ACID (UNII: 6VT1YZM21H)
- COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A)
- DISODIUM COCOYL GLUTAMATE (UNII: MBK0CP8F5A)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- ORANGE OIL (UNII: AKN3KSD11B)
- GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
- CHENOPODIUM QUINOA SEED (UNII: OO4K72NZ2X)
- ALCOHOL (UNII: 3K9958V90M)
- BENZYL ACETATE (UNII: 0ECG3V79ZJ)
- CAPRYLOYL GLYCERIN/SEBACIC ACID COPOLYMER (2000 MPA.S) (UNII: N7YC58165T)
What is the NDC to RxNorm Crosswalk for J1002901jason Dandruff Relief 2in1treatment?
- RxCUI: 209884 - zinc pyrithione 1 % Medicated Shampoo
- RxCUI: 209884 - zinc pyrithione 10 MG/ML Medicated Shampoo
- RxCUI: 209884 - zinc pyrithione 1 % Medicated Conditioner
* Please review the disclaimer below.
[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".