NDC 54340-003 Dial For Men Dandruff Control Hair And Body Wash
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
YELLOW (C48330 - YELLOW 5)
Code Structure Chart
Product Details
What is NDC 54340-003?
What are the uses for Dial For Men Dandruff Control Hair And Body Wash?
Which are Dial For Men Dandruff Control Hair And Body Wash 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 Dial For Men Dandruff Control Hair And Body Wash 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)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- CARBOMER 1342 (UNII: 809Y72KV36)
- GLYCERIN (UNII: PDC6A3C0OX)
- LAURETH-7 (UNII: Z95S6G8201)
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
What is the NDC to RxNorm Crosswalk for Dial For Men Dandruff Control Hair And Body Wash?
- RxCUI: 1091088 - zinc pyrithione 0.95 % Medicated Shampoo
- RxCUI: 1091088 - zinc pyrithione 9.5 MG/ML Medicated Shampoo
- RxCUI: 1091092 - Dial Dandruff Control Hair and Body 0.95 % Medicated Shampoo
- RxCUI: 1091092 - zinc pyrithione 9.5 MG/ML Medicated Shampoo [Dial Dandruff Control]
- RxCUI: 1091092 - Dial Dandruff Control 9.5 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".