NDC 67172-174 Chloraseptic Sore Throat Max Liquid Center
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 67172 - Prestige Brands Holdings, Inc.
- 67172-174 - Chloraseptic Sore Throat Max Liquid Center
Product Characteristics
Product Packages
NDC Code 67172-174-61
Package Description: 1 BLISTER PACK in 1 CARTON / 15 LOZENGE in 1 BLISTER PACK
Product Details
What is NDC 67172-174?
What are the uses for Chloraseptic Sore Throat Max Liquid Center?
Which are Chloraseptic Sore Throat Max 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 Max 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 BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- GLYCERIN (UNII: PDC6A3C0OX)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- SUCROSE (UNII: C151H8M554)
- WATER (UNII: 059QF0KO0R)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
What is the NDC to RxNorm Crosswalk for Chloraseptic Sore Throat Max Liquid Center?
- RxCUI: 1046351 - benzocaine 15 MG / menthol 10 MG Oral Lozenge
- RxCUI: 1046353 - Chloraseptic Max Sore Throat 10 MG / 15 MG Oral Lozenge
- RxCUI: 1046353 - benzocaine 15 MG / menthol 10 MG Oral Lozenge [Chloraseptic Sore Throat]
- RxCUI: 1046353 - Chloraseptic Sore Throat Max (benzocaine 15 MG / menthol 10 MG) Oral Lozenge
- RxCUI: 1046353 - Chloraseptic Sore Throat Max Oral Lozenge
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[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".