NDC 64942-3785 Axe Acne Control 2% Salicylic Acid
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 64942 - Conopco, Inc. D/b/a/ Unilever
- 64942-3785 - Axe Acne Control 2% Salicylic Acid
Product Packages
NDC Code 64942-3785-8
Package Description: 127.5 g in 1 CARTON
Product Details
What is NDC 64942-3785?
What are the uses for Axe Acne Control 2% Salicylic Acid?
Which are Axe Acne Control 2% Salicylic Acid UNII Codes?
The UNII codes for the active ingredients in this product are:
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Axe Acne Control 2% Salicylic Acid 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:
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- TURMERIC (UNII: 856YO1Z64F)
- EXT. D&C YELLOW NO. 7 (UNII: 08F8S9O3I5)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- WATER (UNII: 059QF0KO0R)
- SODIUM GLUCONATE (UNII: R6Q3791S76)
- PARSLEY (UNII: 58FMD0Q0EV)
- GLYCERIN (UNII: PDC6A3C0OX)
- SODIUM PALM KERNELATE (UNII: 6H91L1NXTW)
- PALM ACID (UNII: B6G0Y5Z616)
- SODIUM PALMATE (UNII: S0A6004K3Z)
- PALM KERNEL ACID (UNII: 79P21R4317)
- MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K)
- FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)
What is the NDC to RxNorm Crosswalk for Axe Acne Control 2% Salicylic Acid?
- RxCUI: 562600 - salicylic acid 2 % Medicated Liquid Soap
- RxCUI: 562600 - salicylic acid 20 MG/ML Medicated Liquid Soap
- RxCUI: 562600 - salicylic acid 2 % Facial Cleanser Toner
- RxCUI: 562600 - salicylic acid 2 % Facial Scrub
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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".