NDC 12546-314 Hallssugar Free Extra Sugar Free Extra Strong Menthol
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 12546 - Mondelez Global Llc
- 12546-314 - Hallssugar Free Extra
Product Characteristics
Product Packages
NDC Code 12546-314-09
Package Description: 9 LOZENGE in 1 PACKAGE
Product Details
What is NDC 12546-314?
What are the uses for Hallssugar Free Extra Sugar Free Extra Strong Menthol?
Which are Hallssugar Free Extra Sugar Free Extra Strong Menthol UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Hallssugar Free Extra Sugar Free Extra Strong Menthol 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:
- ACESULFAME POTASSIUM (UNII: 23OV73Q5G9)
- ASPARTAME (UNII: Z0H242BBR1)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- ISOMALT (UNII: S870P55O2W)
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Hallssugar Free Extra Sugar Free Extra Strong Menthol?
- RxCUI: 1422187 - Menthol 18 MG Oral Lozenge
- RxCUI: 1422187 - menthol 18 MG Oral Lozenge
- RxCUI: 1422189 - Halls 18 MG Oral Lozenge
- RxCUI: 1422189 - menthol 18 MG Oral Lozenge [Halls]
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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".