NDC 43596-0004 Lbel Renovance Jour Daytime Face Spf 15 All Skin Types
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43596 - Ventura Corporation, Ltd
- 43596-0004 - Lbel Renovance Jour Daytime Face Spf 15 All Skin Types
Product Packages
NDC Code 43596-0004-0
Package Description: 1 g in 1 POUCH
NDC Code 43596-0004-1
Package Description: 5 g in 1 JAR
NDC Code 43596-0004-2
Package Description: 50 g in 1 JAR
Product Details
What is NDC 43596-0004?
What are the uses for Lbel Renovance Jour Daytime Face Spf 15 All Skin Types?
Which are Lbel Renovance Jour Daytime Face Spf 15 All Skin Types 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 Renovance Jour Daytime Face Spf 15 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)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- GLYCERIN (UNII: PDC6A3C0OX)
- PEA (UNII: W4X7H8GYFM)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
- MANNITOL (UNII: 3OWL53L36A)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PEG-75 STEARATE (UNII: OT38R0N74H)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CARBOMER INTERPOLYMER TYPE A (55000 MPA.S) (UNII: 59TL3WG5CO)
- TROLAMINE (UNII: 9O3K93S3TK)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- PANTHENOL (UNII: WV9CM0O67Z)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- CETETH-20 (UNII: I835H2IHHX)
- STEARETH-20 (UNII: L0Q8IK9E08)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TEPRENONE (UNII: S8S8451A4O)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- EDETATE SODIUM (UNII: MP1J8420LU)
- POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- SERINE (UNII: 452VLY9402)
- UREA (UNII: 8W8T17847W)
- HEDERA HELIX LEAF (UNII: ZP9XFG71A7)
- YEAST (UNII: 3NY3SM6B8U)
- CHLORELLA VULGARIS (UNII: RYQ4R60M02)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ZINC PIDOLATE (UNII: C32PQ86DH4)
- ALLANTOIN (UNII: 344S277G0Z)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- ACACIA (UNII: 5C5403N26O)
- 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".