NDC 49825-117 Bioelements, Inc. Spf 50 Facescreen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 49825 - Bioelements, Inc.
- 49825-117 - Bioelements, Inc.
Product Packages
NDC Code 49825-117-02
Package Description: 1 JAR in 1 BOX / 73 mL in 1 JAR (49825-117-01)
Product Details
What is NDC 49825-117?
What are the uses for Bioelements, Inc. Spf 50 Facescreen?
Which are Bioelements, Inc. Spf 50 Facescreen UNII Codes?
The UNII codes for the active ingredients in this product are:
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Bioelements, Inc. Spf 50 Facescreen 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)
- ALOE (UNII: V5VD430YW9)
- GLYCERIN (UNII: PDC6A3C0OX)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ASIAN GINSENG (UNII: CUQ3A77YXI)
- CENTELLA ASIATICA (UNII: 7M867G6T1U)
- ANGELICA SINENSIS ROOT (UNII: B66F4574UG)
- RORIPPA NASTURTIUM-AQUATICUM (UNII: YH89GMV676)
- RHUS GLABRA BARK (UNII: 7XC0E9WP6U)
- CHAMOMILE (UNII: FGL3685T2X)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIETHANOLAMINE CETYL PHOSPHATE (UNII: 4UG0316V9S)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- TROLAMINE (UNII: 9O3K93S3TK)
- CARBOMER 934 (UNII: Z135WT9208)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- GLYCERETH-2 COCOATE (UNII: JWM00VS7HC)
- IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
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[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".