NDC 62742-4189 Gentle Hydrating Sunscreen Broad Spectrum Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 62742 - Allure Labs Inc
- 62742-4189 - Gentle Hydrating Sunscreen Broad Spectrum Spf 30
Product Packages
NDC Code 62742-4189-1
Package Description: 57 g in 1 TUBE
Product Details
What is NDC 62742-4189?
What are the uses for Gentle Hydrating Sunscreen Broad Spectrum Spf 30?
Which are Gentle Hydrating Sunscreen Broad Spectrum Spf 30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Gentle Hydrating 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)
- COCONUT ALKANES (UNII: 1E5KJY107T)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- GLYCERIN (UNII: PDC6A3C0OX)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- COCO GLUCOSIDE (UNII: ICS790225B)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- CAPRYLYL/CAPRYL OLIGOGLUCOSIDE (UNII: E00JL9G9K0)
- APPLE (UNII: B423VGH5S9)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- SHEANUT (UNII: 84H6HBP32L)
- HYDROLYZED JOJOBA ESTERS (ACID FORM) (UNII: UDR641JW8W)
- COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
- GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- POLYGLYCERYL-3 RICINOLEATE (UNII: MZQ63P0N0W)
- ISOSTEARIC ACID (UNII: X33R8U0062)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- HEXASODIUM PHYTATE (UNII: ZBX50UG81V)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- XANTHAN GUM (UNII: TTV12P4NEE)
- TOCOPHEROL (UNII: R0ZB2556P8)
- BETASIZOFIRAN (UNII: 2X51AD1X3T)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
* 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".