NDC 69435-1606 Mineralium Hdra Source Moisturizing Protector Spf 25
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 69435-1606?
Which are Mineralium Hdra Source Moisturizing Protector Spf 25 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
Which are Mineralium Hdra Source Moisturizing Protector Spf 25 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)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- GLYCERIN (UNII: PDC6A3C0OX)
- SIMMONDSIA CHINENSIS SEED (UNII: D24K2Q1F6H)
- SHEA BUTTER (UNII: K49155WL9Y)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- NIACINAMIDE (UNII: 25X51I8RD4)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- SEA SALT (UNII: 87GE52P74G)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- PANTHENOL (UNII: WV9CM0O67Z)
- CHAMOMILE FLOWER OIL (UNII: 60F80Z61A9)
- POMEGRANATE SEED OIL (UNII: 0UI45XV0T6)
- CAMELINA SATIVA WHOLE (UNII: W42JFE4HON)
* 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".