NDC 68016-407 Premier Value Cold Sore Treatment
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68016 - Premier Value
- 68016-407 - Premier Value Cold Sore Treatment
Product Packages
NDC Code 68016-407-01
Package Description: 1 TUBE in 1 PACKAGE / 2 g in 1 TUBE
Product Details
What is NDC 68016-407?
What are the uses for Premier Value Cold Sore Treatment?
Which are Premier Value Cold Sore Treatment UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (Active Moiety)
Which are Premier Value Cold Sore Treatment 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:
- ALCOHOL (UNII: 3K9958V90M)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ARGININE (UNII: 94ZLA3W45F)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- CERESIN (UNII: Q1LS2UJO3A)
- CETEARYL ISONONANOATE (UNII: P5O01U99NI)
- CORYMBIA CITRIODORA LEAF OIL (UNII: M63U6N96EB)
- DIPROPYLENE GLYCOL CAPRATE/CAPRYLATE DIESTER (UNII: R6G12EY23X)
- ETHYLPARABEN (UNII: 14255EXE39)
- HEXYLDECANOL (UNII: 151Z7P1317)
- HEXYLDECYL LAURATE (UNII: 0V595C1P6M)
- LEVOMENTHOL (UNII: BZ1R15MTK7)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLOXAMER 407 (UNII: TUF2IVW3M2)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- TEA TREE OIL (UNII: VIF565UC2G)
- THYMOL (UNII: 3J50XA376E)
- TOCOPHERYL NICOTINATE, D-.ALPHA. (UNII: WI1J5UCY5C)
- ZINC CHLORIDE (UNII: 86Q357L16B)
What is the NDC to RxNorm Crosswalk for Premier Value Cold Sore Treatment?
- RxCUI: 1374851 - benzalkonium chloride 0.13 % / camphor 3 % Topical Cream
- RxCUI: 1374851 - benzalkonium chloride 1.3 MG/ML / camphor 30 MG/ML Topical Cream
* 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".