NDC 13537-995 Lbel Lederm 35 Plus Jour Facial Against First Signs Of Aging
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 13537-995?
What are the uses for Lbel Lederm 35 Plus Jour Facial Against First Signs Of Aging?
Which are Lbel Lederm 35 Plus Jour Facial Against First 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 35 Plus Jour Facial Against First 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)
- 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)
- XANTHAN GUM (UNII: TTV12P4NEE)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- ACACIA (UNII: 5C5403N26O)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- YEAST, UNSPECIFIED (UNII: 3NY3SM6B8U)
- PRUNUS PERSICA LEAF (UNII: VN3501T41P)
- GLYCERIN (UNII: PDC6A3C0OX)
- CAROB (UNII: 5MG5Z946UO)
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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".