NDC 76348-441 Acne Control Body Wash
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 76348 - Renu Laboratories Inc.
- 76348-441 - Acne Control Body Wash
Product Packages
NDC Code 76348-441-02
Package Description: 1 TUBE in 1 BOX / 168 g in 1 TUBE (76348-441-01)
Product Details
What is NDC 76348-441?
What are the uses for Acne Control Body Wash?
Which are Acne Control Body Wash 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 Control Body 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:
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- GLYCOLIC ACID (UNII: 0WT12SX38S)
- TOCOPHEROL (UNII: R0ZB2556P8)
- ALOE (UNII: V5VD430YW9)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- CHAMOMILE (UNII: FGL3685T2X)
- CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- CITRIC ACID ACETATE (UNII: DSO12WL7AU)
- ACRYLIC ACID/ISOPHORONE DIISOCYANATE/PEG-27 COPOLYMER (UNII: R0R8I3X29J)
- SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
What is the NDC to RxNorm Crosswalk for Acne Control Body Wash?
- 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".