TUSSIN COUGH EXPECTORANT COUGH SUPRESSANT 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: TUSSIN COUGH EXPECTORANT COUGH SUPRESSANT DM
Generic name: DEXTROMETHORPHAN HYDROBROMIDE
Manufacturer: AptaPharma Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 8a4c55d0-c472-4e89-9fdb-17ecf0af4856
SPL ID: 5b440237-78c8-458a-b365-8b77ae10fdd3
Version: 5
Effective date: 2023-12-30
Source export date: 2026-09-28
Source partition: 9
Source file: https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/6784607726c827491ceaeab30d843632e0660ee8008c535197be5ed9e1e52201/drug-label-0009-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:03:18

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		M012	openfda.application_number
brand name		TUSSIN COUGH EXPECTORANT COUGH SUPRESSANT DM	openfda.brand_name
generic name		DEXTROMETHORPHAN HYDROBROMIDE	openfda.generic_name
manufacturer name		AptaPharma Inc.	openfda.manufacturer_name
ndc	package	76281-503-24	openfda.package_ndc
ndc	product	76281-503	openfda.product_ndc
ndc11	package	76281050324	derived:openfda.package_ndc
rxcui		996520	openfda.rxcui
spl id		5b440237-78c8-458a-b365-8b77ae10fdd3	id
spl set id		8a4c55d0-c472-4e89-9fdb-17ecf0af4856	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 ■ in a child under 12 years of age ■ if you are now taking aprescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric or emotional conditions, or Parkinson's disease) or for 2 weeks atter stopping the MAOI drug. If you do not know if your prescription drug contains a MAOI, ask adoctor or pharmacist before using this product.

Reported adverse events (FAERS/openFDA)#

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