NDC 53175-004 Hcs Roll-on Antiperspirant
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 53175-004?
What are the uses for Hcs Roll-on Antiperspirant?
Which are Hcs Roll-on Antiperspirant UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M)
- ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (Active Moiety)
Which are Hcs Roll-on Antiperspirant 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)
- MINERAL OIL (UNII: T5L8T28FGP)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
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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".