NDC 55910-220 All Day Allergy Relief 24 Hour
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 55910 - Dolgencorp, Inc. (dollar General & Rexall)
- 55910-220 - All Day Allergy Relief
Product Characteristics
Product Packages
NDC Code 55910-220-14
Package Description: 1 BLISTER PACK in 1 CARTON / 14 TABLET in 1 BLISTER PACK
Product Details
What is NDC 55910-220?
What are the uses for All Day Allergy Relief 24 Hour?
Which are All Day Allergy Relief 24 Hour UNII Codes?
The UNII codes for the active ingredients in this product are:
- CETIRIZINE HYDROCHLORIDE (UNII: 64O047KTOA)
- CETIRIZINE (UNII: YO7261ME24) (Active Moiety)
Which are All Day Allergy Relief 24 Hour 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:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
- POVIDONES (UNII: FZ989GH94E)
- SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- POLYVINYL ALCOHOL (UNII: 532B59J990)
- STARCH, CORN (UNII: O8232NY3SJ)
- TALC (UNII: 7SEV7J4R1U)
What is the NDC to RxNorm Crosswalk for All Day Allergy Relief 24 Hour?
- RxCUI: 1014678 - cetirizine HCl 10 MG Oral Tablet
- RxCUI: 1014678 - cetirizine hydrochloride 10 MG Oral Tablet
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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".