NDC 0311-0585 Almay Sensitive Skin Antiperspirant - Deodorant Roll-on Fragrance Free
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 0311 - Almay, Inc
- 0311-0585 - Almay Sensitive Skin Antiperspirant - Deodorant
Product Packages
NDC Code 0311-0585-97
Package Description: 50 mL in 1 BOTTLE, WITH APPLICATOR
Product Details
What is NDC 0311-0585?
What are the uses for Almay Sensitive Skin Antiperspirant - Deodorant Roll-on Fragrance Free?
Which are Almay Sensitive Skin Antiperspirant - Deodorant Roll-on Fragrance Free 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 Almay Sensitive Skin Antiperspirant - Deodorant Roll-on Fragrance Free 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)
- DI-PPG-2 MYRETH-10 ADIPATE (UNII: 4IN301M0KJ)
- LAURETH-23 (UNII: N72LMW566G)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- LAURETH-4 (UNII: 6HQ855798J)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- LAURIC ACID (UNII: 1160N9NU9U)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- BEHENTRIMONIUM METHOSULFATE (UNII: 5SHP745C61)
- EDETIC ACID (UNII: 9G34HU7RV0)
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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".