Refenesen 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: Refenesen Mucus Relief DM
Generic name: DEXTROMETHORPHAN HYDROBROMIDE / GUAIFENESIN
Manufacturer: Reese Pharmaceutical Co
Product type: HUMAN OTC DRUG
SPL set ID: 6046dc50-f162-4e2d-aa3c-7d27efad477d
SPL ID: 05d6a014-cf43-4f17-afd9-014267e1d9ff
Version: 5
Effective date: 2024-12-18
Source export date: 2026-09-28
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:24:38

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 · 14 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M012	openfda.application_number
brand name		Refenesen Mucus Relief DM	openfda.brand_name
generic name		DEXTROMETHORPHAN HYDROBROMIDE / GUAIFENESIN	openfda.generic_name
manufacturer name		Reese Pharmaceutical Co	openfda.manufacturer_name
ndc	package	10956-846-50	openfda.package_ndc
ndc	package	10956-846-30	openfda.package_ndc
ndc	product	10956-846	openfda.product_ndc
ndc11	package	10956084650	derived:openfda.package_ndc
ndc11	package	10956084630	derived:openfda.package_ndc
rxcui		1147685	openfda.rxcui
spl id		05d6a014-cf43-4f17-afd9-014267e1d9ff	id
spl set id		6046dc50-f162-4e2d-aa3c-7d27efad477d	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 ■ if you are now taking a prescription monoamine oxidase (inhiMor~MAIO) (Certain drugs for depression, psychiatric or emotional conditioners or Parkinson's disease)or for 2 weeks after stopping MAIO drug, If you do not know if your prescription drug contains an MAIO, ask your doctor or pharmacist before using this product.

Reported adverse events (FAERS/openFDA)#

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