NDC 66163-0603 Liage - Mineral Rich Tinted Sunscreen Broad Spectrum Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 66163 - Cosmetic Solutions Llc
- 66163-0603 - Liage - Mineral Rich Tinted Sunscreen Broad Spectrum Spf 30
Product Packages
NDC Code 66163-0603-1
Package Description: 1 BOTTLE in 1 CARTON / 60 mL in 1 BOTTLE
Product Details
What is NDC 66163-0603?
What are the uses for Liage - Mineral Rich Tinted Sunscreen Broad Spectrum Spf 30?
Which are Liage - Mineral Rich Tinted 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 Liage - Mineral Rich Tinted 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)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- GLYCERIN (UNII: PDC6A3C0OX)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- COCOYL CAPRYLOCAPRATE (UNII: 8D9H4QU99H)
- ALUMINUM STEARATE (UNII: U6XF9NP8HM)
- CARTHAMUS TINCTORIUS SEED OLEOSOMES (UNII: 9S60Q72309)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- POLYGONUM AVICULARE TOP (UNII: ZCD6009IUF)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- GARDEN CRESS SPROUT (UNII: PWQ18YNR62)
- SQUALANE (UNII: GW89575KF9)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
- COCO GLUCOSIDE (UNII: ICS790225B)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- DOCOSANOL (UNII: 9G1OE216XY)
- XANTHAN GUM (UNII: TTV12P4NEE)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ)
- JOJOBA OIL (UNII: 724GKU717M)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- SUCROSE STEARATE (UNII: 274KW0O50M)
- PHENYLETHYL ALCOHOL (UNII: ML9LGA7468)
- TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
- GLYCERYL MONOCAPRYLATE (UNII: TM2TZD4G4A)
- SORBITAN MONOOLEATE (UNII: 06XEA2VD56)
- POLYGLYCERYL-2 CAPRATE (UNII: JX7WXJ41DH)
- PROPANEDIOL (UNII: 5965N8W85T)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
* 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".