55629-015 NDC - ACETAMINOPHEN, GUAIFENESIN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL ()

Drug Information

Product NDC: 55629-015

Proprietary Name: Acetaminophen, Guaifenesin, Dextromethorphan HBr, Phenylephrine HCl

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: ONE2ZEE LIMITED LIABILITY COMPANY
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:3/1/2021

Package Information

No. Package Code Package Description Billing Unit
155629-015-0148 POUCH in 1 CARTON (55629-015-01) / 300 CAPSULE, LIQUID FILLED in 1 POUCH (55629-015-02)

NDC Record

Field Name Field Value Definition
PRODUCT NDC55629-015The 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 NAMEAcetaminophen, Guaifenesin, Dextromethorphan HBr, Phenylephrine HClThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE3/1/2021This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEONE2ZEE LIMITED LIABILITY 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