NDC 53863-124 Clarifying Line Broad Spectrum Spf 50 Exel
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53863 - Exelencia Importers
- 53863-124 - Clarifying Line Broad Spectrum Spf 50
Product Packages
NDC Code 53863-124-02
Package Description: 1 TUBE in 1 CARTON / 100 mL in 1 TUBE (53863-124-01)
Product Details
What is NDC 53863-124?
What are the uses for Clarifying Line Broad Spectrum Spf 50 Exel?
Which are Clarifying Line Broad Spectrum Spf 50 Exel UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Clarifying Line Broad Spectrum Spf 50 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:
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- SHEANUT OIL (UNII: O88E196QRF)
- EDETATE CALCIUM DISODIUM ANHYDROUS (UNII: 8U5D034955)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- CYCLOMETHICONE (UNII: NMQ347994Z)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE (UNII: ANQ870JD20)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- ECTOINE (UNII: 7GXZ3858RY)
- GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
- HAMAMELIS VIRGINIANA TOP (UNII: UDA30A2JJY)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- WATER (UNII: 059QF0KO0R)
- XANTHAN GUM (UNII: TTV12P4NEE)
- YEAST, UNSPECIFIED (UNII: 3NY3SM6B8U)
* 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".