NDC 62742-4086 Spf 30 Mineral Sunscreen Face Neck
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 62742 - Allure Labs Inc
- 62742-4086 - Spf 30 Mineral Sunscreen Face Neck
Product Packages
NDC Code 62742-4086-1
Package Description: 2 mL in 1 TUBE
NDC Code 62742-4086-3
Package Description: 1 TUBE in 1 CARTON / 50 mL in 1 TUBE (62742-4086-2)
Product Details
What is NDC 62742-4086?
What are the uses for Spf 30 Mineral Sunscreen Face Neck?
Which are Spf 30 Mineral Sunscreen Face Neck UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
Which are Spf 30 Mineral Sunscreen Face Neck 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)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PEG-100 STEARATE (UNII: YD01N1999R)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- POLYGLYCERYL-3 POLYDIMETHYLSILOXYETHYL DIMETHICONE (4000 MPA.S) (UNII: RLA2U05Z4Q)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- SHEA BUTTER (UNII: K49155WL9Y)
- POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
- PHYSALIS ANGULATA (UNII: W4TKW9D5GG)
- TEPRENONE (UNII: S8S8451A4O)
- LEONTOPODIUM ALPINUM FLOWERING TOP (UNII: QQC1AK06RK)
- POLYGONUM AVICULARE TOP (UNII: ZCD6009IUF)
- IMPERATA CYLINDRICA ROOT (UNII: VYT2JA85NH)
- ARABIDOPSIS THALIANA (UNII: AI3L60HQ81)
- CAMELLIA SINENSIS FLOWER (UNII: 9I2BJY2J17)
- PHOENIX RECLINATA FRUIT (UNII: B140O227ZE)
- SODIUM LACTATE (UNII: TU7HW0W0QT)
- PALMITOYL TRIPEPTIDE-1 (UNII: RV743D216M)
- PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- LAURETH-7 (UNII: Z95S6G8201)
- XANTHAN GUM (UNII: TTV12P4NEE)
- CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
- 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".