NDC 12546-985 Halls Plus Strawberry
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Product Details
What is NDC 12546-985?
What are the uses for Halls Plus Strawberry?
Which are Halls Plus Strawberry UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Halls Plus Strawberry 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:
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- GLYCERIN (UNII: PDC6A3C0OX)
- POTASSIUM CITRATE (UNII: EE90ONI6FF)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- SUCROSE (UNII: C151H8M554)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Halls Plus Strawberry?
- RxCUI: 1250183 - Halls 2.7 MG Oral Lozenge
- RxCUI: 1250183 - menthol 2.7 MG Oral Lozenge [Halls]
- RxCUI: 433196 - menthol 2.7 MG 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".