Maximum Strength Mucus DM Extended Release

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Maximum Strength Mucus DM Extended Release
Generic name: GUAIFENESIN AND DEXTROMETHORPHAN HBR
Manufacturer: CVS Pharmacy, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 5ea560d1-6443-4271-842c-7801fc6a6043
SPL ID: 9d11e2a3-e3be-4bf8-b556-b8af9ee9c234
Version: 8
Effective date: 2025-08-11
Source export date: 2026-10-30
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-30/023bc8d8aae5addb7530087bbbdb169b3ccbf36764f15b8ca67db07e1e5aea8b/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run: 20261102T182004Z
Imported at: 2026-11-02 19:10:08

Harmonized routes table
Harmonized routes
ORAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 17 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application applno	ANDA	206941	derived:openfda.application_number
application number		ANDA206941	openfda.application_number
brand name		Maximum Strength Mucus DM Extended Release	openfda.brand_name
generic name		GUAIFENESIN AND DEXTROMETHORPHAN HBR	openfda.generic_name
manufacturer name		CVS Pharmacy, Inc.	openfda.manufacturer_name
ndc	package	69842-059-65	openfda.package_ndc
ndc	package	69842-059-10	openfda.package_ndc
ndc	package	69842-059-70	openfda.package_ndc
ndc	product	69842-059	openfda.product_ndc
ndc11	package	69842005965	derived:openfda.package_ndc
ndc11	package	69842005970	derived:openfda.package_ndc
ndc11	package	69842005910	derived:openfda.package_ndc
rxcui		1099074	openfda.rxcui
spl id		9d11e2a3-e3be-4bf8-b556-b8af9ee9c234	id
spl set id		5ea560d1-6443-4271-842c-7801fc6a6043	set_id
unii		9D2RTI9KYH	openfda.unii
unii		495W7451VQ	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings Do not use for children under 12 years of age if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric or emotional conditions, or Parkinson’s disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.