NDC 64483-378 Estro-lift Day Therapy Moisturizer And Spf 30 Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
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Product Details
What is NDC 64483-378?
What are the uses for Estro-lift Day Therapy Moisturizer And Spf 30 Sunscreen?
Which are Estro-lift Day Therapy Moisturizer And Spf 30 Sunscreen UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Estro-lift Day Therapy Moisturizer And Spf 30 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)
- GLYCOL STEARATE SE (UNII: 6YLY96TQL6)
- PPG-30 CETYL ETHER (UNII: 00C2W8NVII)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- DIHEXADECYL PHOSPHATE (UNII: 2V6E5WN99N)
- CETETH-10 PHOSPHATE (UNII: 4E05O5N49G)
- DIETHANOLAMINE CETYL PHOSPHATE (UNII: 4UG0316V9S)
- DISODIUM ACETYL GLUCOSAMINE PHOSPHATE (UNII: SC89MF712W)
- SACCHARIDE ISOMERATE (UNII: W8K377W98I)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CENTELLA ASIATICA (UNII: 7M867G6T1U)
- ECHINACEA PURPUREA (UNII: QI7G114Y98)
- SQUALANE (UNII: GW89575KF9)
- PANTHENOL (UNII: WV9CM0O67Z)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- NELUMBO NUCIFERA SEED (UNII: YCT65RT6AE)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- PINUS STROBUS BARK (UNII: 8PJ4761097)
- VITIS VINIFERA SEED (UNII: C34U15ICXA)
- GLYCERIN (UNII: PDC6A3C0OX)
- CATALASE (BOS TAURUS) (UNII: A7I0CI22DA)
- SUPEROXIDE DISMUTASE (SACCHAROMYCES CEREVISIAE) (UNII: W2T4YRA9AD)
- CYCLOMETHICONE (UNII: NMQ347994Z)
- SODIUM CARBOXYMETHYL .BETA.-GLUCAN (DS 0.65-0.85) (UNII: 2YGO1190AP)
- MAGNESIUM ASCORBYL PHOSPHATE (UNII: 0R822556M5)
- SOYBEAN (UNII: L7HT8F1ZOD)
- UBIDECARENONE (UNII: EJ27X76M46)
- SOY ISOFLAVONES (UNII: 71B37NR06D)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- CHOLECALCIFEROL (UNII: 1C6V77QF41)
- BETA CAROTENE (UNII: 01YAE03M7J)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- HYDROXYETHYL ETHYLCELLULOSE (UNII: ZDN57Z154K)
- EDETATE SODIUM (UNII: MP1J8420LU)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
* 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".