NDC 13537-990 Lbel Defense Total Broad Spectrum Spf 50plus Sunscreen For Face And Body
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 13537 - Ventura Corporation Ltd
- 13537-990 - Lbel Defense Total Broad Spectrum Spf 50plus Sunscreen For Face And Body
Product Packages
NDC Code 13537-990-01
Package Description: 120 mL in 1 BOTTLE, PLASTIC
NDC Code 13537-990-02
Package Description: 80 mL in 1 BOTTLE, PLASTIC
NDC Code 13537-990-04
Package Description: 1 TUBE in 1 BOX / 10 mL in 1 TUBE (13537-990-03)
NDC Code 13537-990-05
Package Description: 5 mL in 1 PACKET
NDC Code 13537-990-06
Package Description: 1 mL in 1 PACKET
NDC Code 13537-990-08
Package Description: 1 PACKET in 1 CARTON / .07 mL in 1 PACKET (13537-990-07)
Product Details
What is NDC 13537-990?
What are the uses for Lbel Defense Total Broad Spectrum Spf 50plus Sunscreen For Face And Body?
Which are Lbel Defense Total Broad Spectrum Spf 50plus Sunscreen For Face And Body UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Lbel Defense Total Broad Spectrum Spf 50plus Sunscreen For Face And Body 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)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8)
- PHENETHYL BENZOATE (UNII: 0C143929GK)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CETYL PALMITATE (UNII: 5ZA2S6B08X)
- HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)
- PHYSALIS ANGULATA (UNII: W4TKW9D5GG)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)
- XANTHAN GUM (UNII: TTV12P4NEE)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- OXOTHIAZOLIDINE (UNII: M6U1ZG59XD)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
* 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".