NDC 59779-806 Viper Acne Body Wash
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 59779 - Cvs Pharmacy
- 59779-806 - Viper Acne Body Wash
Product Packages
NDC Code 59779-806-12
Package Description: 354 mL in 1 BOTTLE
Product Details
What is NDC 59779-806?
What are the uses for Viper Acne Body Wash?
Which are Viper Acne 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 Viper Acne 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:
- WATER (UNII: 059QF0KO0R)
- SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- SODIUM C12-15 PARETH-15 SULFONATE (UNII: 353VA59XH8)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- LINOLEAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: 5Q87K461JO)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- 1-DECENE (UNII: 7O4U4C718P)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CHAMAEMELUM NOBILE FLOWER (UNII: O2T154T6OG)
- CHAMOMILE (UNII: FGL3685T2X)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- EXT. D&C VIOLET NO. 2 (UNII: G5UX3K0728)
What is the NDC to RxNorm Crosswalk for Viper Acne 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".