NDC 10477-7720 Daily Moisturizing Antioxidant Spf 50
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 10477 - Goodier Cosmetics Llc
- 10477-7720 - Daily Moisturizing Antioxidant Spf 50
Product Packages
NDC Code 10477-7720-1
Package Description: 1 TUBE in 1 CARTON / 48 g in 1 TUBE
NDC Code 10477-7720-2
Package Description: 227 g in 1 TUBE
NDC Code 10477-7720-3
Package Description: 3 g in 1 TUBE
Product Details
What is NDC 10477-7720?
What are the uses for Daily Moisturizing Antioxidant Spf 50?
Which are Daily Moisturizing Antioxidant Spf 50 UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
Which are Daily Moisturizing Antioxidant Spf 50 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)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- BORON NITRIDE (UNII: 2U4T60A6YD)
- SORBITOL (UNII: 506T60A25R)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PEG-100 STEARATE (UNII: YD01N1999R)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
- YEAST (UNII: 3NY3SM6B8U)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- EPIGALLOCATECHIN GALLATE (UNII: BQM438CTEL)
- BETULA PUBESCENS BARK (UNII: 3R504894L9)
- BIOSACCHARIDE GUM-1 (UNII: BB4PU4V09H)
- UBIDECARENONE (UNII: EJ27X76M46)
- CETYL DIMETHICONE 25 (UNII: U4AS1BW4ZB)
- PALMITOYL TRIPEPTIDE-5 (UNII: 2A3916MQHO)
- SQUALANE (UNII: GW89575KF9)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- PALMITOYLLYSYLVALYLDIAMINOBUTYROYLTHREONINE (UNII: 1615WE9073)
- POMEGRANATE (UNII: 56687D1Z4D)
- STEARETH-20 (UNII: L0Q8IK9E08)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ALLANTOIN (UNII: 344S277G0Z)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- TOCOPHEROL (UNII: R0ZB2556P8)
- STEARETH-10 (UNII: FD0913P475)
- SIMMONDSIA CHINENSIS SEED (UNII: D24K2Q1F6H)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
- 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".