NDC 71084-001 Alkmene Anti Spot Pad
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 71084-001?
What are the uses for Alkmene Anti Spot Pad?
Which are Alkmene Anti Spot Pad UNII Codes?
The UNII codes for the active ingredients in this product are:
- TEA TREE OIL (UNII: VIF565UC2G)
- TEA TREE OIL (UNII: VIF565UC2G) (Active Moiety)
Which are Alkmene Anti Spot Pad 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)
- ALCOHOL (UNII: 3K9958V90M)
- ALLANTOIN (UNII: 344S277G0Z)
- GLYCERIN (UNII: PDC6A3C0OX)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- TOCOPHEROL (UNII: R0ZB2556P8)
- MANUKA OIL (UNII: M6QU9ZUH2X)
- CARBOMER 934 (UNII: Z135WT9208)
- MAGNOLIA GRANDIFLORA BARK (UNII: J4XF5T6418)
- NIGELLA SATIVA SEED OIL (UNII: CS4U38E731)
- ACRYLAMIDE (UNII: 20R035KLCI)
- HYDROGENATED PALM GLYCERIDES (UNII: YCZ8EM144Q)
- POTASSIUM LAURATE (UNII: V4361R8N4Z)
- AMINO ACIDS (UNII: 0O72R8RF8A)
- LECITHIN, SUNFLOWER (UNII: 834K0WOS5G)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- .ALPHA.-(.ALPHA.-AMINOPROPYL)BENZYL ALCOHOL (UNII: S8TT5K3C8Y)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
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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".