NDC 14783-038 Lbel Paris Renovance Jour
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 14783 - Ventura International Ltd
- 14783-038 - Lbel Paris
Product Packages
NDC Code 14783-038-61
Package Description: 1 JAR in 1 BOX / 50 g in 1 JAR (14783-038-62)
Product Details
What is NDC 14783-038?
What are the uses for Lbel Paris Renovance Jour?
Which are Lbel Paris Renovance Jour UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Lbel Paris Renovance Jour 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)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- GLYCERIN (UNII: PDC6A3C0OX)
- SNOW PEA (UNII: 84SKC33B1I)
- C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
- MANNITOL (UNII: 3OWL53L36A)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- TROLAMINE (UNII: 9O3K93S3TK)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- PANTHENOL (UNII: WV9CM0O67Z)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- STEARETH-20 (UNII: L0Q8IK9E08)
- CETETH-20 (UNII: I835H2IHHX)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TEPRENONE (UNII: S8S8451A4O)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
- EDETATE SODIUM (UNII: MP1J8420LU)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- KALMIA LATIFOLIA LEAF (UNII: 79N6542N18)
- YEAST (UNII: 3NY3SM6B8U)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- SERINE (UNII: 452VLY9402)
- UREA (UNII: 8W8T17847W)
- ACACIA (UNII: 5C5403N26O)
- ALLANTOIN (UNII: 344S277G0Z)
- SODIUM SUCCINATE ANHYDROUS (UNII: V8ZGC8ISR3)
* 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".