NDC 58479-040 Sport Natural Mineral Sunscreen Broad Spectrum Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 58479 - Crossing Cultures Llc Dba Goddess Garden
- 58479-040 - Sport Natural Mineral Sunscreen Broad Spectrum
Product Packages
NDC Code 58479-040-00
Package Description: 28 g in 1 TUBE
NDC Code 58479-040-01
Package Description: 96 g in 1 TUBE
NDC Code 58479-040-02
Package Description: 6 g in 1 PACKET
Product Details
What is NDC 58479-040?
What are the uses for Sport Natural Mineral Sunscreen Broad Spectrum Spf 30?
Which are Sport Natural Mineral Sunscreen Broad Spectrum Spf 30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Sport Natural 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- SHEA BUTTER (UNII: K49155WL9Y)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
- SAFFLOWER OIL (UNII: 65UEH262IS)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)
- GLYCERYL STEARATE CITRATE (UNII: WH8T92A065)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- TOCOPHEROL (UNII: R0ZB2556P8)
- XANTHAN GUM (UNII: TTV12P4NEE)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- SORBITAN MONOOLEATE (UNII: 06XEA2VD56)
- WATER (UNII: 059QF0KO0R)
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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".