NDC 58479-206 Kids 50 Spf50
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 58479 - Crossing Cultures Llc Dba Goddess Garden
- 58479-206 - Kids 50
Product Packages
NDC Code 58479-206-02
Package Description: 100 g in 1 TUBE
Product Details
What is NDC 58479-206?
What are the uses for Kids 50 Spf50?
Which are Kids 50 Spf50 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 Kids 50 Spf50 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:
- CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
- SAFFLOWER OIL (UNII: 65UEH262IS)
- GLYCERIN (UNII: PDC6A3C0OX)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- SORBITAN MONOOLEATE (UNII: 06XEA2VD56)
- TOCOPHEROL (UNII: R0ZB2556P8)
- WATER (UNII: 059QF0KO0R)
- GLYCERYL MONOCAPRYLATE (UNII: TM2TZD4G4A)
- GLYCERYL STEARATE CITRATE (UNII: WH8T92A065)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- XANTHAN GUM (UNII: TTV12P4NEE)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- SHEA BUTTER (UNII: K49155WL9Y)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- LAVANDIN OIL (UNII: 9RES347CKG)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
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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".