NDC 58443-0420 Coretex Broad Spectrum Spf 30 Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 58443 - Prime Enterprises Inc.
- 58443-0420 - Coretex
Product Characteristics
Product Packages
NDC Code 58443-0420-1
Package Description: 18927 mL in 1 CONTAINER
Product Details
What is NDC 58443-0420?
What are the uses for Coretex Broad Spectrum Spf 30 Sunscreen?
Which are Coretex Broad Spectrum Spf 30 Sunscreen 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)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
Which are Coretex Broad Spectrum Spf 30 Sunscreen 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:
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- SORBITAN MONOOLEATE (UNII: 06XEA2VD56)
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
- COCOA BUTTER (UNII: 512OYT1CRR)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- WATER (UNII: 059QF0KO0R)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
* 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".