NDC 42851-186 Zo Skin Health Skin Normalizing System With Rozatrol Booster Serum
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 42851-186?
What are the uses for Zo Skin Health Skin Normalizing System With Rozatrol Booster Serum?
Which are Zo Skin Health Skin Normalizing System With Rozatrol Booster Serum 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 Zo Skin Health Skin Normalizing System With Rozatrol Booster Serum 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:
- ALCOHOL (UNII: 3K9958V90M)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- CRITHMUM MARITIMUM (UNII: J7IHY79BKY)
- GLYCOLIC ACID (UNII: 0WT12SX38S)
- HAMAMELIS VIRGINIANA TOP (UNII: UDA30A2JJY)
- BARLEY (UNII: 5PWM7YLI7R)
- MANDELIC ACID (UNII: NH496X0UJX)
- MENTHYL LACTATE, (-)- (UNII: 2BF9E65L7I)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- PLANTAGO LANCEOLATA LEAF (UNII: 2YWL9J7EE8)
- PTEROCARPUS SOYAUXII WOOD (UNII: 0V6QB4C61P)
- ROSA CANINA FRUIT (UNII: 3TNW8D08V3)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- UREA (UNII: 8W8T17847W)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Zo Skin Health Skin Normalizing System With Rozatrol Booster Serum?
- RxCUI: 1546588 - salicylic acid 2 % Medicated Patch
- RxCUI: 1546588 - salicylic acid 0.02 MG/MG Medicated Patch
- RxCUI: 797892 - salicylic acid 2 % Medicated Pad
- RxCUI: 797892 - salicylic acid 20 MG/ML Medicated Pad
- RxCUI: 797892 - salicylic acid 2 % Topical Swab
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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".