0363-9891 NDC - MUCUS RELIEF DM ()

Drug Information

Product NDC: 0363-9891

Proprietary Name: MUCUS RELIEF DM

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Walgreens
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:8/15/2015

Package Information

No. Package Code Package Description Billing Unit
10363-9891-1414 PLASTER in 1 BOX (0363-9891-14)
20363-9891-303 BLISTER PACK in 1 CARTON (0363-9891-30) / 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

NDC Record

Field Name Field Value Definition
PRODUCT NDC0363-9891The 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 NAMEMUCUS RELIEF DMThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE8/15/2015This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEWalgreensName of Company corresponding to the labeler code segment of the Product NDC.
PRODUCT NDC0363-9891The 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 NAMESalicylic AcidThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE5/20/2011This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEWalgreens CompanyName 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