NDC 62742-4181 Self Reflect Probiotic Sunscreen Moisturizer Broad Spectrum Spf 32
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 62742 - Allure Labs Inc
- 62742-4181 - Self Reflect Probiotic Sunscreen Moisturizer Broad Spectrum Spf 32
Product Packages
NDC Code 62742-4181-2
Package Description: 1 TUBE in 1 CARTON / 50 g in 1 TUBE (62742-4181-1)
Product Details
What is NDC 62742-4181?
What are the uses for Self Reflect Probiotic Sunscreen Moisturizer Broad Spectrum Spf 32?
Which are Self Reflect Probiotic Sunscreen Moisturizer Broad Spectrum Spf 32 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 Self Reflect Probiotic Sunscreen Moisturizer Broad Spectrum Spf 32 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)
- APPLE (UNII: B423VGH5S9)
- COCO GLUCOSIDE (UNII: ICS790225B)
- LACTOBACILLUS REUTERI (UNII: 9913I24QEE)
- RASPBERRY SEED OIL (UNII: 9S8867952A)
- COCONUT WATER (UNII: 267F5Y81NT)
- TURMERIC OIL (UNII: 6KGS8SP16U)
- SHEANUT (UNII: 84H6HBP32L)
- HYDROLYZED JOJOBA ESTERS (ACID FORM) (UNII: UDR641JW8W)
- TOCOPHEROL (UNII: R0ZB2556P8)
- GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
- VANILLA (UNII: Q74T35078H)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- ISOSTEARIC ACID (UNII: X33R8U0062)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- POLYGLYCERYL-3 RICINOLEATE (UNII: MZQ63P0N0W)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
- CAPRYLYL/CAPRYL OLIGOGLUCOSIDE (UNII: E00JL9G9K0)
- BETASIZOFIRAN (UNII: 2X51AD1X3T)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- XANTHAN GUM (UNII: TTV12P4NEE)
- OCTYLDODECANOL (UNII: 461N1O614Y)
- STARCH, TAPIOCA (UNII: 24SC3U704I)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- SORBITAN MONOOLEATE (UNII: 06XEA2VD56)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
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[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".