NDC 70549-123 Antidandruff
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Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 70549-123?
What are the uses for Antidandruff?
Which are Antidandruff 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 Antidandruff 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:
- POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- WATER (UNII: 059QF0KO0R)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- GLYCERIN (UNII: PDC6A3C0OX)
- LAURAMIDOPROPYL BETAINE (UNII: 23D6XVI233)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- PEG-7 GLYCERYL COCOATE (UNII: VNX7251543)
- PEG-200 HYDROGENATED GLYCERYL PALMATE (UNII: W161T051Y1)
- EDETATE SODIUM (UNII: MP1J8420LU)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- PEG/PPG-14/4 DIMETHICONE (UNII: 646XNV22YX)
- PIROCTONE OLAMINE (UNII: A4V5C6R9FB)
- PANTHENOL (UNII: WV9CM0O67Z)
- MENTHOL (UNII: L7T10EIP3A)
- SAGE (UNII: 065C5D077J)
- URTICA DIOICA LEAF (UNII: X6M0DRN46Q)
- MENTHA PIPERITA (UNII: 79M2M2UDA9)
What is the NDC to RxNorm Crosswalk for Antidandruff?
- RxCUI: 209884 - zinc pyrithione 1 % Medicated Shampoo
- RxCUI: 209884 - zinc pyrithione 10 MG/ML Medicated Shampoo
- RxCUI: 209884 - zinc pyrithione 1 % Medicated Conditioner
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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".