NDC 10967-583 Womens Mitchum Advanced Invisible Roll-on Antiperspirant Deodorant Powder Fresh
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 10967 - Revlon Consumer Products Corp
- 10967-583 - Womens Mitchum Advanced Invisible
Product Packages
NDC Code 10967-583-97
Package Description: 50 mL in 1 BOTTLE, WITH APPLICATOR
Product Details
What is NDC 10967-583?
What are the uses for Womens Mitchum Advanced Invisible Roll-on Antiperspirant Deodorant Powder Fresh?
Which are Womens Mitchum Advanced Invisible Roll-on Antiperspirant Deodorant Powder Fresh UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY (UNII: 8O386558JE)
- ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY (UNII: 8O386558JE) (Active Moiety)
Which are Womens Mitchum Advanced Invisible Roll-on Antiperspirant Deodorant 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)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- HYDROGEN PEROXIDE (UNII: BBX060AN9V)
- SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)
- LAURETH-4 (UNII: 6HQ855798J)
- BEHENTRIMONIUM METHOSULFATE (UNII: 5SHP745C61)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- LAURIC ACID (UNII: 1160N9NU9U)
- EDETIC ACID (UNII: 9G34HU7RV0)
- BENZYL SALICYLATE (UNII: WAO5MNK9TU)
- LINALOOL, (+)- (UNII: F4VNO44C09)
- .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
- COUMARIN (UNII: A4VZ22K1WT)
- .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
- GERANIOL (UNII: L837108USY)
* Please review the disclaimer below.
[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".