Cough Relief

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: Cough Relief
Generic name: DEXTROMETHORPHAN HYDROBROMIDE
Manufacturer: Advanced Rx LLC
Product type: HUMAN OTC DRUG
SPL set ID: 297e10e3-e740-4434-91a2-2e5c54985d33
SPL ID: 2bd504ed-3944-e6ce-e063-6294a90aa3de
Version: 1
Effective date: 2025-01-01
Source export date: 2026-09-28
Source partition: 11
Source file: https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:16:02

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 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M012	openfda.application_number
brand name		Cough Relief	openfda.brand_name
generic name		DEXTROMETHORPHAN HYDROBROMIDE	openfda.generic_name
manufacturer name		Advanced Rx LLC	openfda.manufacturer_name
ndc	package	80513-311-06	openfda.package_ndc
ndc	product	80513-311	openfda.product_ndc
ndc11	package	80513031106	derived:openfda.package_ndc
rxcui		1090487	openfda.rxcui
spl id		2bd504ed-3944-e6ce-e063-6294a90aa3de	id
spl set id		297e10e3-e740-4434-91a2-2e5c54985d33	set_id
unii		9D2RTI9KYH	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 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.