NDC 42851-190 Zo Medical 3-step Peel Kit
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 42851-190?
What are the uses for Zo Medical 3-step Peel Kit?
Which are Zo Medical 3-step Peel Kit UNII Codes?
The UNII codes for the active ingredients in this product are:
- OATMEAL (UNII: 8PI54V663Y)
- OATMEAL (UNII: 8PI54V663Y) (Active Moiety)
Which are Zo Medical 3-step Peel Kit 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- PETROLATUM (UNII: 4T6H12BN9U)
- DISTEARYLDIMONIUM CHLORIDE (UNII: OM9573ZX3X)
- ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- SHEA BUTTER (UNII: K49155WL9Y)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11)
- GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- ALCOHOL (UNII: 3K9958V90M)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- DIBENZYL ETHER (UNII: 2O6CNO27RJ)
- TETRAPEPTIDE-21 (UNII: 179JUC43HU)
What is the NDC to RxNorm Crosswalk for Zo Medical 3-step Peel Kit?
- RxCUI: 240464 - colloidal oatmeal 1 % Topical Lotion
- RxCUI: 240464 - colloidal oatmeal 10 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".