NDC 29500-2216 Personal Care Pyrithione Zinc Dandruff
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 29500 - Personal Care Products, Llc
- 29500-2216 - Personal Care Pyrithione Zinc Dandruff
Product Packages
NDC Code 29500-2216-0
Package Description: 400 mL in 1 BOTTLE
Product Details
What is NDC 29500-2216?
What are the uses for Personal Care Pyrithione Zinc Dandruff?
Which are Personal Care Pyrithione Zinc 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 Personal Care Pyrithione Zinc 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 LAURYL SULFATE (UNII: 368GB5141J)
- COCO MONOETHANOLAMIDE (UNII: C80684146D)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- POLYQUATERNIUM-10 (400 CPS AT 2%) (UNII: HB1401PQFS)
- GLYCOL DISTEARATE (UNII: 13W7MDN21W)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
What is the NDC to RxNorm Crosswalk for Personal Care Pyrithione Zinc 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".