MUCUS RELIEF DM

openFDA label record#

Cross-check layer: This is openFDA JSON-derived label data. Use the corresponding DailyMed SPL as the canonical label.

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

Brand name: MUCUS RELIEF DM
Generic name: DEXTROMETHORPHAN HBR/GUAIFENESIN
Manufacturer: KROGER COMPANY
Product type: HUMAN OTC DRUG
SPL set ID: 813baf42-edb0-33a9-e053-2a91aa0a8599
SPL ID: 89697bdd-6c45-47bf-e053-2a95a90aa0ca
Version: 2
Effective date: 2019-05-21
Source export date: 2026-08-01
Source partition: 7
Source file: https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-08-01/29baabee7fa6726d72190670d84f1571113181a958a8119cbe97e8f0d1d955b2/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run: 20260801T225920Z
Imported at: 2026-08-01 23:13:34

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 · 12 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		part341	openfda.application_number
brand name		MUCUS RELIEF DM	openfda.brand_name
generic name		DEXTROMETHORPHAN HBR/GUAIFENESIN	openfda.generic_name
manufacturer name		KROGER COMPANY	openfda.manufacturer_name
ndc	package	41226-280-03	openfda.package_ndc
ndc	product	41226-280	openfda.product_ndc
ndc11	package	41226028003	derived:openfda.package_ndc
rxcui		1147685	openfda.rxcui
spl id		89697bdd-6c45-47bf-e053-2a95a90aa0ca	id
spl set id		813baf42-edb0-33a9-e053-2a91aa0a8599	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 · 2 matching rows.

warnings

WARNINGS: Do not use 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.

warnings table

<table border="0" width="100%"> <tbody> <tr> <td>WARNINGS: Do not use 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.</td> </tr> </tbody> </table>