NDC 13537-448 Lbel Lederm 55plus Jour Spf 15 Facial Treatment Against Advanced Signs Of Aging Day - All Skin Types
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 13537 - Ventura Corporation Ltd.
- 13537-448 - Lbel Lederm 55plus Jour
Product Packages
NDC Code 13537-448-01
Package Description: 1 g in 1 PACKET
NDC Code 13537-448-04
Package Description: 1 BOTTLE, PLASTIC in 1 BOX / 5 g in 1 BOTTLE, PLASTIC (13537-448-03)
NDC Code 13537-448-06
Package Description: 1 BOTTLE, GLASS in 1 BOX / 50 g in 1 BOTTLE, GLASS (13537-448-05)
Product Details
What is NDC 13537-448?
What are the uses for Lbel Lederm 55plus Jour Spf 15 Facial Treatment Against Advanced Signs Of Aging Day - All Skin Types?
Which are Lbel Lederm 55plus Jour Spf 15 Facial Treatment Against Advanced Signs Of Aging Day - 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 Lbel Lederm 55plus Jour Spf 15 Facial Treatment Against Advanced Signs Of Aging Day - 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)
- 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)
- CETETH-20 (UNII: I835H2IHHX)
- STEARETH-20 (UNII: L0Q8IK9E08)
- EDETATE SODIUM (UNII: MP1J8420LU)
- ACACIA (UNII: 5C5403N26O)
- CHICORY ROOT (UNII: 090CTY533N)
- ALARIA ESCULENTA (UNII: EJ9JK8J58D)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- ALCOHOL (UNII: 3K9958V90M)
- FOLIC ACID (UNII: 935E97BOY8)
* 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".