NDC 69842-666 Foamimg Acne Face Wash
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69842 - Cvs
- 69842-666 - Foamimg Acne Face Wash
Product Packages
NDC Code 69842-666-05
Package Description: 187 g in 1 TUBE
Product Details
What is NDC 69842-666?
Which are Foamimg Acne Face Wash UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZOYL PEROXIDE (UNII: W9WZN9A0GM)
- BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (Active Moiety)
Which are Foamimg Acne Face Wash 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:
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCOLIC ACID (UNII: 0WT12SX38S)
- LACTIC ACID (UNII: 33X04XA5AT)
- MINERAL OIL (UNII: T5L8T28FGP)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POTASSIUM LAURYL PHOSPHATE (UNII: C4QT53N4MK)
- SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- SODIUM LAURYL SULFOACETATE (UNII: D0Y70F2B9J)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Foamimg Acne Face Wash?
- RxCUI: 142034 - benzoyl peroxide 10 % Medicated Liquid Soap
- RxCUI: 142034 - benzoyl peroxide 100 MG/ML Medicated Liquid Soap
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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".