NDC 73418-021 Zinc Oxide
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 73418-021?
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:
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- COCONUT OIL (UNII: Q9L0O73W7L)
- CANDELILLA WAX (UNII: WL0328HX19)
- CASTOR OIL (UNII: D5340Y2I9G)
- RASPBERRY SEED OIL (UNII: 9S8867952A)
- APRICOT KERNEL OIL (UNII: 54JB35T06A)
- ARGAN OIL (UNII: 4V59G5UW9X)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- TOCOPHEROL (UNII: R0ZB2556P8)
- ROSA CANINA FRUIT OIL (UNII: CR7307M3QZ)
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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".