NDC 49527-992 Acne Solutions Cleansing Foam
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 49527-992?
What are the uses for Acne Solutions Cleansing Foam?
Which are Acne Solutions Cleansing Foam 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 Acne Solutions Cleansing Foam 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- SODIUM METHYL COCOYL TAURATE (UNII: JVL98CG53G)
- SUCROSE (UNII: C151H8M554)
- SACCHARINA LATISSIMA THALLUS (UNII: 68CMP2MB55)
- COLA NUT (UNII: PQM9SA369U)
- CAFFEINE (UNII: 3G6A5W338E)
- PEPPERMINT (UNII: V95R5KMY2B)
- PSEUDOPTEROGORGIA ELISABETHAE (UNII: UDY3H1OUX5)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- STEARAMIDOPROPYL DIMETHYLAMINE (UNII: K7VEI00UFR)
- N-ACETYLGLUCOSAMINE (UNII: V956696549)
- CAPRYLOYL GLYCINE (UNII: 8TY5YO42NJ)
- PERILLALDEHYDE (UNII: 6EQL0XA86G)
- 10-HYDROXYDECANOIC ACID (UNII: NP03XO416B)
- CARYOPHYLLENE (UNII: BHW853AU9H)
- SODIUM STEARATE (UNII: QU7E2XA9TG)
- SODIUM SALICYLATE (UNII: WIQ1H85SYP)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CHLOROXYLENOL (UNII: 0F32U78V2Q)
What is the NDC to RxNorm Crosswalk for Acne Solutions Cleansing Foam?
- 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".