NDC 51060-293 Tarteguard 30 Sunscreen Broad Spectrum Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 51060 - Tarte, Inc.
- 51060-293 - Tarteguard 30 Sunscreen Broad Spectrum Spf 30
Product Packages
NDC Code 51060-293-01
Package Description: 1 BOTTLE, PUMP in 1 CARTON / 13 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 51060-293?
Which are Tarteguard 30 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 Tarteguard 30 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)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- COCOYL CAPRYLOCAPRATE (UNII: 8D9H4QU99H)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- DIHEPTYL SUCCINATE (UNII: 057N7SS26Y)
- POLYGLYCERYL-6 DISTEARATE (UNII: Z35I17EQOP)
- PROPANEDIOL (UNII: 5965N8W85T)
- HYDROGENATED JOJOBA OIL, RANDOMIZED (UNII: Q47ST02F58)
- GLYCERIN (UNII: PDC6A3C0OX)
- APPLE (UNII: B423VGH5S9)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- DIETHYLHEXYL SYRINGYLIDENEMALONATE (UNII: 3V5U97P248)
- XANTHAN GUM (UNII: TTV12P4NEE)
- TOCOPHEROL (UNII: R0ZB2556P8)
- SOYBEAN OIL (UNII: 241ATL177A)
- CAPRYLOYL GLYCERIN/SEBACIC ACID COPOLYMER (2000 MPA.S) (UNII: N7YC58165T)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- LONICERA CAPRIFOLIUM FLOWER (UNII: 5N1WD9784U)
- TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- PASSIFLORA EDULIS SEED OIL (UNII: F3VOA31UHQ)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)
- GERANIOL (UNII: L837108USY)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- SODIUM SALICYLATE (UNII: WIQ1H85SYP)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
* Please review the disclaimer below.
[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".