NDC 36800-309 Dandruff
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 36800 - Topco Associates Llc
- 36800-309 - Dandruff
Product Packages
NDC Code 36800-309-13
Package Description: 420 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 36800-309?
What are the uses for Dandruff?
Which are Dandruff 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 Dandruff 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)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- GLYCOL DISTEARATE (UNII: 13W7MDN21W)
- ZINC CARBONATE (UNII: EQR32Y7H0M)
- SODIUM XYLENESULFONATE (UNII: G4LZF950UR)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A)
- MAGNESIUM CARBONATE HYDROXIDE (UNII: YQO029V1L4)
- MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
What is the NDC to RxNorm Crosswalk for Dandruff?
- 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".