NDC 62742-4079 Spf 30 Body Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 62742 - Alure Labs, Inc.
- 62742-4079 - Spf 30 Body Sunscreen
Product Packages
NDC Code 62742-4079-2
Package Description: 1 TUBE in 1 CARTON / 120 mL in 1 TUBE (62742-4079-1)
Product Details
What is NDC 62742-4079?
What are the uses for Spf 30 Body Sunscreen?
Which are Spf 30 Body Sunscreen UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Spf 30 Body 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)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- GLYCERIN (UNII: PDC6A3C0OX)
- SORBITAN MONOOLEATE (UNII: 06XEA2VD56)
- UBIDECARENONE (UNII: EJ27X76M46)
- PHYSALIS ANGULATA (UNII: W4TKW9D5GG)
- TEPRENONE (UNII: S8S8451A4O)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- ACTINIDIA CHINENSIS ROOT (UNII: 1L6O0O338I)
- ARTEMISIA VULGARIS ROOT (UNII: 32MP823R8S)
- CENTELLA ASIATICA (UNII: 7M867G6T1U)
- ECHINACEA PURPUREA (UNII: QI7G114Y98)
- PALMITOYL PENTAPEPTIDE-4 (UNII: KK181SM5JG)
- LEONTOPODIUM ALPINUM FLOWER (UNII: MWN6IZU3XM)
- ARABIDOPSIS THALIANA (UNII: AI3L60HQ81)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- POLYGONUM AVICULARE TOP (UNII: ZCD6009IUF)
- XANTHAN GUM (UNII: TTV12P4NEE)
- EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)
- CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 809Y72KV36)
- CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- TROLAMINE (UNII: 9O3K93S3TK)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- TOCOPHEROL (UNII: R0ZB2556P8)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
* 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".