NDC 53863-120 Sunscreen Creme Spf 37 Exel
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53863 - Exelencia Importers Corp
- 53863-120 - Sunscreen Creme Spf 37
Product Packages
NDC Code 53863-120-02
Package Description: 1 BOTTLE in 1 CARTON / 50 mL in 1 BOTTLE (53863-120-01)
Product Details
What is NDC 53863-120?
What are the uses for Sunscreen Creme Spf 37 Exel?
Which are Sunscreen Creme Spf 37 Exel 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)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Sunscreen Creme Spf 37 Exel 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)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- HAMAMELIS VIRGINIANA TOP (UNII: UDA30A2JJY)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- SHEA BUTTER (UNII: K49155WL9Y)
- XANTHAN GUM (UNII: TTV12P4NEE)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- TROLAMINE (UNII: 9O3K93S3TK)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
* 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".