NDC 13537-026 Lbel Protege Expert
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 13537 - Ventura Corporation Ltd.
- 13537-026 - Lbel
Product Packages
NDC Code 13537-026-02
Package Description: 1 TUBE in 1 BOX / 5 mL in 1 TUBE (13537-026-01)
NDC Code 13537-026-04
Package Description: 1 TUBE in 1 BOX / 10 mL in 1 TUBE (13537-026-03)
NDC Code 13537-026-06
Package Description: 1 BOTTLE in 1 BOX / 180 mL in 1 BOTTLE (13537-026-05)
Product Details
What is NDC 13537-026?
What are the uses for Lbel Protege Expert?
Which are Lbel Protege Expert UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Lbel Protege Expert 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)
- DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- TROLAMINE (UNII: 9O3K93S3TK)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- XANTHAN GUM (UNII: TTV12P4NEE)
- MANNITOL (UNII: 3OWL53L36A)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- ETHYLPARABEN (UNII: 14255EXE39)
- ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
- ARGININE (UNII: 94ZLA3W45F)
- YEAST (UNII: 3NY3SM6B8U)
- HISTIDINE MONOHYDROCHLORIDE (UNII: 1D5Q932XM6)
- PEA (UNII: W4X7H8GYFM)
- SODIUM SUCCINATE ANHYDROUS (UNII: V8ZGC8ISR3)
- KHAYA SENEGALENSIS BARK (UNII: 1S7EDA839L)
- NADIDE (UNII: 0U46U6E8UK)
- PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)
- ASPARTIC ACID (UNII: 30KYC7MIAI)
* 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".