NDC 82751-103 Zinc Oxide
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What is NDC 82751-103?
What are the uses for Zinc Oxide?
Which are Zinc Oxide UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Zinc Oxide 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:
- CASTOR OIL (UNII: D5340Y2I9G)
- SHEA BUTTER (UNII: K49155WL9Y)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)
- WATER O-18 (UNII: 7QV8F8BYNJ)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
- XANTHAN GUM (UNII: TTV12P4NEE)
- JOJOBA OIL (UNII: 724GKU717M)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
What is the NDC to RxNorm Crosswalk for Zinc Oxide?
- RxCUI: 865073 - zinc oxide 25 % Topical Spray
- RxCUI: 865073 - zinc oxide 250 MG/ML Topical Spray
- RxCUI: 865073 - ZNO 250 MG/ML Topical Spray
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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".