NDC 59779-811 Cvs Deep Cleansing Astringent
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 59779 - Cvs Pharmacy
- 59779-811 - Cvs Deep Cleansing Astringent
Product Packages
NDC Code 59779-811-31
Package Description: 250 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 59779-811?
What are the uses for Cvs Deep Cleansing Astringent?
Which are Cvs Deep Cleansing Astringent 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 Cvs Deep Cleansing Astringent 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)
- ALCOHOL (UNII: 3K9958V90M)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- BENZOPHENONE (UNII: 701M4TTV9O)
- DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)
- LAURAMIDOPROPYL BETAINE (UNII: 23D6XVI233)
- GLYCERIN (UNII: PDC6A3C0OX)
- ISOCETYL ALCOHOL (UNII: 1800H64066)
- PEG-32 STEARATE (UNII: 33GX5WQC0M)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
What is the NDC to RxNorm Crosswalk for Cvs Deep Cleansing Astringent?
- RxCUI: 199308 - salicylic acid 0.5 % Topical Solution
- RxCUI: 199308 - salicylic acid 5 MG/ML Topical Solution
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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".