NDC 81901-001 Eb Epicurus Spf 50 The Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 81901 - Biocrown Biotechnology Co., Ltd
- 81901-001 - Eb Epicurus Spf 50 The Sunscreen
Product Packages
NDC Code 81901-001-35
Package Description: 35 mL in 1 BOTTLE
Product Details
What is NDC 81901-001?
What are the uses for Eb Epicurus Spf 50 The Sunscreen?
Which are Eb Epicurus Spf 50 The Sunscreen UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
Which are Eb Epicurus Spf 50 The 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:
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- ALCOHOL (UNII: 3K9958V90M)
- POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69)
- MINERAL OIL (UNII: T5L8T28FGP)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
- POLYACRYLIC ACID (8000 MW) (UNII: 73861X4K5F)
- 2,4,6,8-TETRAMETHYLTETRAPHENYLCYCLOTETRASILOXANE, (2.ALPHA.,4.ALPHA.,6.BETA.,8.BETA.)- (UNII: 2F641J843Q)
- PHOSPHATIDYLCHOLINE, SOYBEAN (UNII: 1T6N4D9YV6)
- PPG-3 MYRISTYL ETHER (UNII: 7913J43WZ5)
- CYCLOMETHICONE 4 (UNII: CZ227117JE)
- WATER (UNII: 059QF0KO0R)
- SQUALANE (UNII: GW89575KF9)
- PPG-1 TRIDECETH-6 (UNII: 1K7417JX6Q)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- TRIISOSTEARIN (UNII: 71503RH8KG)
- DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- SODIUM LACTATE (UNII: TU7HW0W0QT)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- GLYCERIN (UNII: PDC6A3C0OX)
- DIOSPYROS KAKI LEAF (UNII: Q71GF9OBNO)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- SORBITAN MONOLAURATE (UNII: 6W9PS8B71J)
- CRANBERRY JUICE (UNII: Y74M3X3345)
- .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
- CUCUMBER (UNII: YY7C30VXJT)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SODIUM ACRYLATE (UNII: 7C98FKB43H)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
* 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".