NDC 13537-426 Lbel Homme Antidandruff
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 13537-426?
What are the uses for Lbel Homme Antidandruff?
Which are Lbel Homme 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 Lbel Homme 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:
- WATER (UNII: 059QF0KO0R)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- COCO DIETHANOLAMIDE (UNII: 92005F972D)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- GLYCOL DISTEARATE (UNII: 13W7MDN21W)
- TROLAMINE (UNII: 9O3K93S3TK)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- COCO GLUCOSIDE (UNII: ICS790225B)
- TEA-DODECYLBENZENESULFONATE (UNII: 8HM7ZD48HN)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- MAGNESIUM NITRATE (UNII: 77CBG3UN78)
- MENTHYL PYRROLIDONE CARBOXYLATE, (-),DL- (UNII: 8P18J856U2)
- ZINC CHLORIDE (UNII: 86Q357L16B)
- GLYCERIN (UNII: PDC6A3C0OX)
- POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
- MENTHOL (UNII: L7T10EIP3A)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- APIGENIN (UNII: 7V515PI7F6)
- OLEANOLIC ACID (UNII: 6SMK8R7TGJ)
- MORINGA OLEIFERA SEED (UNII: TIX5482832)
- BIOTINOYL TRIPEPTIDE-1 (UNII: O6380721VA)
What is the NDC to RxNorm Crosswalk for Lbel Homme Antidandruff?
- RxCUI: 1242513 - zinc pyrithione 0.336 % Medicated Shampoo
- RxCUI: 1242513 - zinc pyrithione 3.36 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".