NDC 59779-343 Advanced Acne Spot Treatment Cvs
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 59779-343?
What are the uses for Advanced Acne Spot Treatment Cvs?
Which are Advanced Acne Spot Treatment Cvs 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 Advanced Acne Spot Treatment Cvs 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)
- HAMAMELIS VIRGINIANA TOP WATER (UNII: NT00Y05A2V)
- GLYCERIN (UNII: PDC6A3C0OX)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- LAURETH-7 (UNII: Z95S6G8201)
- C12-15 ALKYL LACTATE (UNII: GC844VRD7E)
- CETYL LACTATE (UNII: A7EVH2RK4O)
- CEDRUS ATLANTICA BARK (UNII: ITP1Q41UPF)
- CINNAMON BARK OIL (UNII: XE54U569EC)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CAPRYLOYL GLYCINE (UNII: 8TY5YO42NJ)
- AMMONIA (UNII: 5138Q19F1X)
- PURSLANE (UNII: M6S840WXG5)
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- DEHYDROXANTHAN GUM (UNII: 63ZP7I1BQO)
- DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- PPG-2 ISOCETETH-20 ACETATE (UNII: BI6C7YO419)
- SARCOSINE (UNII: Z711V88R5F)
- TERT-BUTYL ALCOHOL (UNII: MD83SFE959)
- EDETATE SODIUM (UNII: MP1J8420LU)
- COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)
What is the NDC to RxNorm Crosswalk for Advanced Acne Spot Treatment Cvs?
- RxCUI: 103568 - salicylic acid 2 % Topical Lotion
- RxCUI: 103568 - salicylic acid 20 MG/ML Topical Lotion
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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".