NDC 13537-754 Lbel Lederm 55 Plus Jour Facial Against Advanced Signs Of Aging
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 13537 - Ventura Corporation Ltd
- 13537-754 - Lbel Lederm 55 Plus Jour Facial Against Advanced Signs Of Aging
Product Packages
NDC Code 13537-754-02
Package Description: 1 BOTTLE in 1 BOX / 50 mL in 1 BOTTLE (13537-754-01)
Product Details
What is NDC 13537-754?
What are the uses for Lbel Lederm 55 Plus Jour Facial Against Advanced Signs Of Aging?
Which are Lbel Lederm 55 Plus Jour Facial Against Advanced Signs Of Aging 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 55 Plus Jour Facial Against Advanced Signs Of Aging 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
- PHENETHYL BENZOATE (UNII: 0C143929GK)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- TRILAURETH-4 PHOSPHATE (UNII: M96W2OLL2V)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- HYDROGENATED PALM GLYCERIDES (UNII: YCZ8EM144Q)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- ALBIZIA JULIBRISSIN BARK (UNII: 0J9G6W44DV)
- PEG-75 STEARATE (UNII: OT38R0N74H)
- XANTHAN GUM (UNII: TTV12P4NEE)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- CETETH-20 (UNII: I835H2IHHX)
- STEARETH-20 (UNII: L0Q8IK9E08)
- EDETATE SODIUM (UNII: MP1J8420LU)
- ACACIA (UNII: 5C5403N26O)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- CHICORY ROOT (UNII: 090CTY533N)
- ALARIA ESCULENTA (UNII: EJ9JK8J58D)
- ALCOHOL (UNII: 3K9958V90M)
- FOLIC ACID (UNII: 935E97BOY8)
- 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".