11822-2112 NDC - RITE AID DAYTIME SEVERE COLD AND COUGH RELIEF ()

Drug Information

Product NDC: 11822-2112

Proprietary Name: Rite Aid Daytime Severe Cold and Cough Relief

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Rite Aid Corporation
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:6/28/2013

Package Information

No. Package Code Package Description Billing Unit
111822-2112-76 POWDER, FOR SOLUTION in 1 CARTON (11822-2112-7)

NDC Record

Field Name Field Value Definition
PRODUCT NDC11822-2112The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAMERite Aid Daytime Severe Cold and Cough ReliefThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE6/28/2013This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMERite Aid CorporationName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 2/1/2023