NDC 80778-008 Sunshine Skin Tint Broad Spectrum Spf 30 - Refill
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 80778 - Milk Makeup Llc
- 80778-008 - Sunshine Skin Tint Broad Spectrum Spf 30 - Refill
Product Characteristics
Product Packages
NDC Code 80778-008-01
Package Description: 1 TUBE in 1 CARTON / 16 mL in 1 TUBE
NDC Code 80778-008-02
Package Description: 1 TUBE in 1 CARTON / 16 mL in 1 TUBE
NDC Code 80778-008-03
Package Description: 1 TUBE in 1 CARTON / 16 mL in 1 TUBE
NDC Code 80778-008-04
Package Description: 1 TUBE in 1 CARTON / 16 mL in 1 TUBE
NDC Code 80778-008-05
Package Description: 1 TUBE in 1 CARTON / 16 mL in 1 TUBE
NDC Code 80778-008-06
Package Description: 1 TUBE in 1 CARTON / 16 mL in 1 TUBE
NDC Code 80778-008-07
Package Description: 1 TUBE in 1 CARTON / 16 mL in 1 TUBE
NDC Code 80778-008-08
Package Description: 1 TUBE in 1 CARTON / 16 mL in 1 TUBE
NDC Code 80778-008-09
Package Description: 1 TUBE in 1 CARTON / 16 mL in 1 TUBE
NDC Code 80778-008-10
Package Description: 1 TUBE in 1 CARTON / 16 mL in 1 TUBE
NDC Code 80778-008-11
Package Description: 1 TUBE in 1 CARTON / 16 mL in 1 TUBE
NDC Code 80778-008-12
Package Description: 1 TUBE in 1 CARTON / 16 mL in 1 TUBE
NDC Code 80778-008-13
Package Description: 1 TUBE in 1 CARTON / 16 mL in 1 TUBE
NDC Code 80778-008-14
Package Description: 1 TUBE in 1 CARTON / 16 mL in 1 TUBE
Product Details
What is NDC 80778-008?
Which are Sunshine Skin Tint Broad Spectrum Spf 30 - Refill UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Sunshine Skin Tint Broad Spectrum Spf 30 - Refill 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:
- HYDROGENATED OLIVE OIL UNSAPONIFIABLES (UNII: B8MIX97W95)
- AVOCADO OIL (UNII: 6VNO72PFC1)
- ISOSTEARIC ACID (UNII: X33R8U0062)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- OLEA EUROPAEA (OLIVE) OIL UNSAPONIFIABLES (UNII: XO45V955LT)
- CRAMBE HISPANICA SUBSP. ABYSSINICA SEED OIL (UNII: 0QW9S92J3K)
- TREMELLA FUCIFORMIS FRUITING BODY (UNII: GG8N28393G)
- LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y)
- JOJOBA OIL (UNII: 724GKU717M)
- GLYCERYL OLEATE (UNII: 4PC054V79P)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- DIISOSTEARYL MALATE (UNII: QBS8A3XZGQ)
- HYDROGENATED JOJOBA OIL, RANDOMIZED (UNII: Q47ST02F58)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- STEARALKONIUM HECTORITE (UNII: OLX698AH5P)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- ACACIA (UNII: 5C5403N26O)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- SQUALANE (UNII: GW89575KF9)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
- POLYGLYCERYL-3 PENTARICINOLEATE (UNII: 7Q0OK5DOT4)
- MANDARIN OIL (UNII: NJO720F72R)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- GRAPE SEED OIL (UNII: 930MLC8XGG)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- TRIBEHENIN (UNII: 8OC9U7TQZ0)
- XANTHAN GUM (UNII: TTV12P4NEE)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- BETAINE (UNII: 3SCV180C9W)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
* 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".