NDC 71398-011 Invisible Shield Full Physical Spf 49 Broad Spectrum Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 71398 - Sent�, Inc.
- 71398-011 - Invisible Shield Full Physical Spf 49 Broad Spectrum Sunscreen
Product Characteristics
Product Packages
NDC Code 71398-011-01
Package Description: 1 TUBE in 1 CARTON / 52 g in 1 TUBE
Product Details
What is NDC 71398-011?
What are the uses for Invisible Shield Full Physical Spf 49 Broad Spectrum Sunscreen?
Which are Invisible Shield Full Physical Spf 49 Broad Spectrum Sunscreen 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 Invisible Shield Full Physical Spf 49 Broad Spectrum Sunscreen 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)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)
- STEARETH-2 (UNII: V56DFE46J5)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- STEARETH-21 (UNII: 53J3F32P58)
- GLYCERIN (UNII: PDC6A3C0OX)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- PROPANEDIOL (UNII: 5965N8W85T)
- BATILOL (UNII: 39YR661C4U)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- XANTHAN GUM (UNII: TTV12P4NEE)
- FRUCTOSE (UNII: 6YSS42VSEV)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- FYTIC ACID (UNII: 7IGF0S7R8I)
- CICHORIUM INTYBUS (CHICORY) ROOT OLIGOSACCHARIDES (UNII: 38AFY41EAR)
- CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- WITHANIA SOMNIFERA ROOT (UNII: V038D626IF)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- YEAST, UNSPECIFIED (UNII: 3NY3SM6B8U)
- BIOSACCHARIDE GUM-4 (UNII: 9XRL057X90)
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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".