Mucus Relief DM

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: Mucus Relief DM
Generic name: GUAIFENESIN AND DEXTROMETHORPHAN HBR
Manufacturer: Ahold U.S.A., Inc,
Product type: HUMAN OTC DRUG
SPL set ID: e9add770-58e0-4cf3-bbc2-d293ca870b03
SPL ID: bab0bd5d-74e4-48cb-9990-6f5944c3d3dc
Version: 5
Effective date: 2023-12-01
Source export date: 2026-10-12
Source partition: 6
Source file: https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/b25dad4aaef9c88f0e827394a34fbbd1ce7d71422fa46b5d1e123befad498c1d/drug-label-0006-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:46:35

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 · 13 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		Mucus Relief DM	openfda.brand_name
generic name		GUAIFENESIN AND DEXTROMETHORPHAN HBR	openfda.generic_name
manufacturer name		Ahold U.S.A., Inc,	openfda.manufacturer_name
ndc	package	60000-058-67	openfda.package_ndc
ndc	product	60000-058	openfda.product_ndc
ndc11	package	60000005867	derived:openfda.package_ndc
rxcui		1298324	openfda.rxcui
spl id		bab0bd5d-74e4-48cb-9990-6f5944c3d3dc	id
spl set id		e9add770-58e0-4cf3-bbc2-d293ca870b03	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.