NDC 14783-014 Lbel Lederm 35plus Jour Spf 15 Facial Treatment Against First Signs Of Aging Day - Oily Skin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 14783 - Ventura International Ltd.
- 14783-014 - Lbel Lederm 35plus Jour
Product Packages
NDC Code 14783-014-01
Package Description: 1 g in 1 PACKET
NDC Code 14783-014-04
Package Description: 1 BOTTLE, PLASTIC in 1 BOX / 5 g in 1 BOTTLE, PLASTIC (14783-014-03)
NDC Code 14783-014-06
Package Description: 1 BOTTLE, GLASS in 1 BOX / 50 g in 1 BOTTLE, GLASS (14783-014-05)
Product Details
What is NDC 14783-014?
What are the uses for Lbel Lederm 35plus Jour Spf 15 Facial Treatment Against First Signs Of Aging Day - Oily Skin?
Which are Lbel Lederm 35plus Jour Spf 15 Facial Treatment Against First Signs Of Aging Day - Oily Skin 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 Lbel Lederm 35plus Jour Spf 15 Facial Treatment Against First Signs Of Aging Day - Oily Skin 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)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- NIACINAMIDE (UNII: 25X51I8RD4)
- PEG-100 STEARATE (UNII: YD01N1999R)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- HYDROGENATED PALM GLYCERIDES (UNII: YCZ8EM144Q)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- XANTHAN GUM (UNII: TTV12P4NEE)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- ACACIA (UNII: 5C5403N26O)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- YEAST (UNII: 3NY3SM6B8U)
- PRUNUS PERSICA LEAF (UNII: VN3501T41P)
- GLYCERIN (UNII: PDC6A3C0OX)
- CAROB (UNII: 5MG5Z946UO)
* 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".