NDC 77069-002 Britto Body Sunscreen Broad Spectrum Spf 50
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 77069 - Mr2 Usa Corporation
- 77069-002 - Britto Body Sunscreen Broad Spectrum Spf 50
Product Characteristics
Product Packages
NDC Code 77069-002-01
Package Description: 100 mL in 1 TUBE
NDC Code 77069-002-02
Package Description: 200 mL in 1 TUBE
Product Details
What is NDC 77069-002?
Which are Britto Body Sunscreen Broad Spectrum Spf 50 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)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Britto Body Sunscreen Broad Spectrum Spf 50 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:
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)
- POTASSIUM STEARATE (UNII: 17V812XK50)
- GLYCERIN (UNII: PDC6A3C0OX)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- EDETATE SODIUM (UNII: MP1J8420LU)
- WATER (UNII: 059QF0KO0R)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- GLYCERYL DIPALMITATE (UNII: 7775E5IR3L)
- GLYCERYL PALMITATE (UNII: 6Y2XJ05B35)
- POLYESTER-7 (UNII: 0841698D2F)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 809Y72KV36)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- XANTHAN GUM (UNII: TTV12P4NEE)
- ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)
- GLYCERYL DISTEARATE (UNII: 73071MW2KM)
* 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".