NDC 52261-4715 Carpe Antiperspirant Underarm Vanilla Scent
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 52261 - Cosco International, Inc.
- 52261-4715 - Carpe Antiperspirant Underarm Vanilla Scent
Product Packages
NDC Code 52261-4715-1
Package Description: .05 kg in 1 TUBE
Product Details
What is NDC 52261-4715?
What are the uses for Carpe Antiperspirant Underarm Vanilla Scent?
Which are Carpe Antiperspirant Underarm Vanilla Scent UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALUMINUM SESQUICHLOROHYDRATE (UNII: UCN889409V)
- ALUMINUM SESQUICHLOROHYDRATE (UNII: UCN889409V) (Active Moiety)
Which are Carpe Antiperspirant Underarm Vanilla Scent 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)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- HEXAMETHYLDISILAZANE (UNII: H36C68P1BH)
- GLYCERIN (UNII: PDC6A3C0OX)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- DIMETHICONE 350 (UNII: 2Y53S6ATLU)
- GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- HYPROMELLOSE 2208 (100000 MPA.S) (UNII: VM7F0B23ZI)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
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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".