NDC 80982-003 Zinc Five-o Spf-50
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 80982 - Astivita Limited
- 80982-003 - Zinc Five-o
Product Packages
NDC Code 80982-003-39
Package Description: 240 g in 1 TUBE
Product Details
What is NDC 80982-003?
What are the uses for Zinc Five-o Spf-50?
Which are Zinc Five-o Spf-50 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
Which are Zinc Five-o Spf-50 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)
- COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
- GLYCERIN (UNII: PDC6A3C0OX)
- COCONUT ALKANES (UNII: 1E5KJY107T)
- JOJOBA OIL (UNII: 724GKU717M)
- POLYGLYCERYL-3 RICINOLEATE (UNII: MZQ63P0N0W)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- ISOSTEARIC ACID (UNII: X33R8U0062)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- PHENYLPROPANOL (UNII: 0F897O3O4M)
- PROPANEDIOL (UNII: 5965N8W85T)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- TOCOPHEROL (UNII: R0ZB2556P8)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- CETYL PHOSPHATE (UNII: VT07D6X67O)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
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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".