NDC 74307-008 Hand Antiperspirant Nightly Use
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 74307-008?
What are the uses for Hand Antiperspirant Nightly Use?
Which are Hand Antiperspirant Nightly Use UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALUMINUM CHLORIDE (UNII: 3CYT62D3GA)
- ALUMINUM CATION (UNII: 3XHB1D032B) (Active Moiety)
Which are Hand Antiperspirant Nightly Use 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:
- POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- GLYCERIN (UNII: PDC6A3C0OX)
- HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP)
- OCTENIDINE HYDROCHLORIDE (UNII: U84956NU4B)
- ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
- COCONUT ALKANES (UNII: 1E5KJY107T)
- COCOYL CAPRYLOCAPRATE (UNII: 8D9H4QU99H)
- WATER (UNII: 059QF0KO0R)
- CETYL HYDROXYETHYLCELLULOSE (350000 MW) (UNII: T7SWE4S2TT)
- TOCOPHEROL (UNII: R0ZB2556P8)
- XANTHAN GUM (UNII: TTV12P4NEE)
- ROSEMARY (UNII: IJ67X351P9)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- RICE BRAN (UNII: R60QEP13IC)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- PROPANEDIOL (UNII: 5965N8W85T)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
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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".