NDC 49825-114 Bioelements Sun Diffusing Protector Spf 15
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 49825 - Bioelements Inc.
- 49825-114 - Bioelements
Product Packages
NDC Code 49825-114-02
Package Description: 1 BOTTLE in 1 BOX / 177 mL in 1 BOTTLE (49825-114-01)
Product Details
What is NDC 49825-114?
What are the uses for Bioelements Sun Diffusing Protector Spf 15?
Which are Bioelements Sun Diffusing Protector Spf 15 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)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Bioelements Sun Diffusing Protector Spf 15 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:
- SORBITOL (UNII: 506T60A25R)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- SAGE OIL (UNII: U27K0H1H2O)
- CITRUS AURANTIUM FRUIT OIL (UNII: 59JDQ5VT0T)
- CITRUS AURANTIUM FLOWER OIL (UNII: D4BGE91OXH)
- IMIDUREA (UNII: M629807ATL)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- TROLAMINE (UNII: 9O3K93S3TK)
* 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".