NDC 50157-009 Crawford Dandruff
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50157 - Brands International
- 50157-009 - Crawford Dandruff
Product Characteristics
Product Packages
NDC Code 50157-009-04
Package Description: 118 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 50157-009?
What are the uses for Crawford Dandruff?
Which are Crawford 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 Crawford 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)
- GLYCOL DISTEARATE (UNII: 13W7MDN21W)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600 KD) (UNII: 0L414VCS5Y)
- EDETATE SODIUM (UNII: MP1J8420LU)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
What is the NDC to RxNorm Crosswalk for Crawford Dandruff?
- RxCUI: 1043014 - zinc pyrithione 0.5 % Medicated Conditioner
- RxCUI: 1043014 - zinc pyrithione 5 MG/ML Medicated Shampoo
- RxCUI: 1043014 - zinc pyrithione 0.5 % Medicated Shampoo
* 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".