NDC 67172-013 Chloraseptic Sore Throat Liquid Center
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 67172 - Prestige Brands Holdings, Inc.
- 67172-013 - Chloraseptic Sore Throat Liquid Center
Product Characteristics
ORANGE (C48331)
YELLOW (C48330)
CITRUS (C73378)
HONEY (C73394)
Product Packages
NDC Code 67172-013-01
Package Description: 1 BLISTER PACK in 1 CARTON / 18 LOZENGE in 1 BLISTER PACK
Product Details
What is NDC 67172-013?
What are the uses for Chloraseptic Sore Throat Liquid Center?
Which are Chloraseptic Sore Throat Liquid Center UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- BENZOCAINE (UNII: U3RSY48JW5)
- BENZOCAINE (UNII: U3RSY48JW5) (Active Moiety)
Which are Chloraseptic Sore Throat Liquid Center 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:
- CORN SYRUP (UNII: 9G5L16BK6N)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- GLYCERIN (UNII: PDC6A3C0OX)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- SUCRALOSE (UNII: 96K6UQ3ZD4)
- WATER (UNII: 059QF0KO0R)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- HONEY (UNII: Y9H1V576FH)
What is the NDC to RxNorm Crosswalk for Chloraseptic Sore Throat Liquid Center?
- RxCUI: 308668 - benzocaine 6 MG / menthol 10 MG Oral Lozenge
- RxCUI: 802559 - Chloraseptic Sore Throat 10 MG / 6 MG Oral Lozenge
- RxCUI: 802559 - benzocaine 6 MG / menthol 10 MG Oral Lozenge [Chloraseptic Sore Throat]
- RxCUI: 802559 - Chloraseptic Sore Throat (benzocaine 6 MG / menthol 10 MG) Oral Lozenge
- RxCUI: 802559 - Chloraseptic Sore Throat Oral Lozenge
* 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".