NDC 14783-119 Lederm Day Sunscreen Broad Spectrum Spf 15 Day Facial Spf 15 Against Noticeable Signs Of Aging All Skin Types
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 14783 - Ventura International
- 14783-119 - Lederm Day Sunscreen Broad Spectrum Spf 15 Day Facial Spf 15 Against Noticeable Signs Of Aging All Skin Types
Product Packages
NDC Code 14783-119-02
Package Description: 1 BOTTLE in 1 BOX / 50 mL in 1 BOTTLE (14783-119-01)
Product Details
What is NDC 14783-119?
What are the uses for Lederm Day Sunscreen Broad Spectrum Spf 15 Day Facial Spf 15 Against Noticeable Signs Of Aging All Skin Types?
Which are Lederm Day Sunscreen Broad Spectrum Spf 15 Day Facial Spf 15 Against Noticeable Signs Of Aging All Skin Types UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Lederm Day Sunscreen Broad Spectrum Spf 15 Day Facial Spf 15 Against Noticeable Signs Of Aging All Skin Types 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)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- GLYCERIN (UNII: PDC6A3C0OX)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- ALBIZIA JULIBRISSIN BARK (UNII: 0J9G6W44DV)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- HYDROGENATED PALM GLYCERIDES (UNII: YCZ8EM144Q)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- XANTHAN GUM (UNII: TTV12P4NEE)
- C20-22 ALKYL PHOSPHATE (UNII: L4VKP0Y7RP)
- C20-22 ALCOHOLS (UNII: O4M0347C6A)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- ACACIA (UNII: 5C5403N26O)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- PALMITOYL LYSYLDIOXYMETHIONYLLYSINE (UNII: T7A529FB8O)
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[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".