NDC 72113-101 Premium Mineral Sunscreen Broad Spectrum Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72113 - Eden Brands
- 72113-101 - Premium Mineral Sunscreen Broad Spectrum Spf 30
Product Packages
NDC Code 72113-101-01
Package Description: 85 g in 1 BOX
Product Details
What is NDC 72113-101?
What are the uses for Premium Mineral Sunscreen Broad Spectrum Spf 30?
Which are Premium Mineral Sunscreen Broad Spectrum Spf 30 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 Premium Mineral Sunscreen Broad Spectrum Spf 30 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)
- WHITE WAX (UNII: 7G1J5DA97F)
- GLYCERYL ISOSTEARATE (UNII: HYE7O27HAO)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- CUCUMBER (UNII: YY7C30VXJT)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- SAFFLOWER OIL (UNII: 65UEH262IS)
- SHEA BUTTER (UNII: K49155WL9Y)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- VITIS VINIFERA SEED (UNII: C34U15ICXA)
- GLYCERIN (UNII: PDC6A3C0OX)
- ROSA CANINA FRUIT OIL (UNII: CR7307M3QZ)
- ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
- CANDELILLA WAX (UNII: WL0328HX19)
- JOJOBA OIL (UNII: 724GKU717M)
- TOCOPHEROL (UNII: R0ZB2556P8)
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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".