NDC 10967-057 Hi And Dri Antiperspirant Roll-on Powder Fresh
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 10967 - Revlon Consumer Products Corp
- 10967-057 - Hi And Dri Antiperspirant
Product Packages
NDC Code 10967-057-97
Package Description: 50 mL in 1 BOTTLE, WITH APPLICATOR
Product Details
What is NDC 10967-057?
What are the uses for Hi And Dri Antiperspirant Roll-on Powder Fresh?
Which are Hi And Dri Antiperspirant Roll-on Powder Fresh 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 Hi And Dri Antiperspirant Roll-on Powder Fresh 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)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- LAURETH-23 (UNII: N72LMW566G)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- LAURETH-4 (UNII: 6HQ855798J)
- LAURIC ACID (UNII: 1160N9NU9U)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- BEHENTRIMONIUM METHOSULFATE (UNII: 5SHP745C61)
- EDETIC ACID (UNII: 9G34HU7RV0)
- ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)
- .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
- GERANIOL (UNII: L837108USY)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- BENZYL SALICYLATE (UNII: WAO5MNK9TU)
- LINALOOL, (+)- (UNII: F4VNO44C09)
- CITRAL (UNII: T7EU0O9VPP)
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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".