NDC 62001-0331 The Original Mane N Tail Daily Control Anti Dandruff
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
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Product Details
What is NDC 62001-0331?
What are the uses for The Original Mane N Tail Daily Control Anti Dandruff?
Which are The Original Mane N Tail Daily Control Anti 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 The Original Mane N Tail Daily Control Anti 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)
- COCO GLUCOSIDE (UNII: ICS790225B)
- CARBOMER INTERPOLYMER TYPE A (55000 MPA.S) (UNII: 59TL3WG5CO)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- PPG-2 HYDROXYETHYL COCAMIDE (UNII: 34N07GUJ3X)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- POLYQUATERNIUM-10 (400 CPS AT 2%) (UNII: HB1401PQFS)
- COCOA BUTTER (UNII: 512OYT1CRR)
- POLYQUATERNIUM-47 (METHACRYLAMIDOPROPYLTRIMETHYLAMMONIUM CHLORIDE-CO-METHYL ACRYLATE-CO-ACRYLIC ACID 45:10:45; 1200000 MW) (UNII: F11YNO8FDQ)
- LAURETH-4 (UNII: 6HQ855798J)
- LAURETH-7 (UNII: Z95S6G8201)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- ALMOND OIL (UNII: 66YXD4DKO9)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- OLEA EUROPAEA LEAF (UNII: MJ95C3OH47)
- EQUISETUM ARVENSE TOP (UNII: 1DP6Y6B65Z)
- LARREA DIVARICATA LEAF (UNII: I15RZ48987)
- TUSSILAGO FARFARA (UNII: 0JXZ63016V)
- HORSE CHESTNUT (UNII: 3C18L6RJAZ)
- FILIPENDULA ULMARIA FLOWER (UNII: 06L18L32G6)
- TRIFOLIUM PRATENSE FLOWER (UNII: 4JS0838828)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
* 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".