NDC 14783-222 Defense Total High Protection Spf 50 No Color Daily Non-greasy Face Protection
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 14783 - Ventura International Ltd
- 14783-222 - Defense Total High Protection Spf 50 No Color Daily Non-greasy Face Protection
Product Packages
NDC Code 14783-222-01
Package Description: 30 mL in 1 BOX
Product Details
What is NDC 14783-222?
What are the uses for Defense Total High Protection Spf 50 No Color Daily Non-greasy Face Protection?
Which are Defense Total High Protection Spf 50 No Color Daily Non-greasy Face Protection UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
Which are Defense Total High Protection Spf 50 No Color Daily Non-greasy Face Protection 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:
- OXOTHIAZOLIDINE (UNII: M6U1ZG59XD)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69)
- XANTHAN GUM (UNII: TTV12P4NEE)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- PHYSALIS ANGULATA WHOLE (UNII: W4TKW9D5GG)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- PHENETHYL BENZOATE (UNII: 0C143929GK)
- VINYLPYRROLIDONE/EICOSENE COPOLYMER (UNII: 035MV9S1C3)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- WATER (UNII: 059QF0KO0R)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN)
- CETYL PALMITATE (UNII: 5ZA2S6B08X)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
* 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".