NDC 77069-003 Britto Facial Sunscreen Broad Spectrum Spf 50
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 77069 - Mr2 Usa Corporation
- 77069-003 - Britto Facial Sunscreen Broad Spectrum Spf 50
Product Packages
NDC Code 77069-003-01
Package Description: 50 mL in 1 TUBE
NDC Code 77069-003-02
Package Description: 100 mL in 1 TUBE
Product Details
What is NDC 77069-003?
What are the uses for Britto Facial Sunscreen Broad Spectrum Spf 50?
Which are Britto Facial 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)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Britto Facial 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:
- WATER (UNII: 059QF0KO0R)
- POTASSIUM STEARATE (UNII: 17V812XK50)
- ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- POLYESTER-7 (UNII: 0841698D2F)
- NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- XANTHAN GUM (UNII: TTV12P4NEE)
- EDETATE SODIUM (UNII: MP1J8420LU)
- GLYCERYL DISTEARATE (UNII: 73071MW2KM)
- GLYCERYL PALMITATE (UNII: 6Y2XJ05B35)
- CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 809Y72KV36)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- GLYCERYL DIPALMITATE (UNII: 7775E5IR3L)
- GLYCERIN (UNII: PDC6A3C0OX)
- PORK COLLAGEN (UNII: I8442U2G7J)
* 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".