NDC 66163-0303 Liage - Herbal Day Cream Broad Spectrum Spf 30 Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 66163 - Cosmetic Solutions Llc
- 66163-0303 - Liage - Herbal Day Cream Broad Spectrum Spf 30 Sunscreen
Product Packages
NDC Code 66163-0303-1
Package Description: 1 JAR in 1 CARTON / 30 g in 1 JAR
Product Details
What is NDC 66163-0303?
What are the uses for Liage - Herbal Day Cream Broad Spectrum Spf 30 Sunscreen?
Which are Liage - Herbal Day Cream Broad Spectrum Spf 30 Sunscreen UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Liage - Herbal Day Cream Broad Spectrum Spf 30 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)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- GLYCERIN (UNII: PDC6A3C0OX)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- STYRENE/ACRYLAMIDE COPOLYMER (500000 MW) (UNII: 5Z4DPO246A)
- COCOYL CAPRYLOCAPRATE (UNII: 8D9H4QU99H)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- CARTHAMUS TINCTORIUS SEED OLEOSOMES (UNII: 9S60Q72309)
- CARDAMOM (UNII: 8BC4CUT4JL)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- PERILLA FRUTESCENS SEED (UNII: 8M62PUD356)
- APPLE (UNII: B423VGH5S9)
- SANTALUM ALBUM SEED (UNII: 7RZT0U509Y)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- CHAMAEMELUM NOBILE FLOWER (UNII: O2T154T6OG)
- CANANGA ODORATA FLOWER (UNII: 76GTF6Z97M)
- ORANGE PEEL (UNII: TI9T76XD44)
- MUSKMELON (UNII: ZV095H5633)
- JASMINUM OFFICINALE FLOWER (UNII: 0Q8K841432)
- LAVANDULA ANGUSTIFOLIA SUBSP. ANGUSTIFOLIA FLOWERING TOP (UNII: 9YT4B71U8P)
- RASPBERRY (UNII: 4N14V5R27W)
- POLYGONUM AVICULARE TOP (UNII: ZCD6009IUF)
- PROPANEDIOL (UNII: 5965N8W85T)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)
- COCO GLUCOSIDE (UNII: ICS790225B)
- HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4)
- DOCOSANOL (UNII: 9G1OE216XY)
- XANTHAN GUM (UNII: TTV12P4NEE)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ)
- PHENYLETHYL ALCOHOL (UNII: ML9LGA7468)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
* 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".