Medique Decorel Forte

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: Medique Decorel Forte
Generic name: ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE
Manufacturer: Unifirst First Aid Corporation
Product type: HUMAN OTC DRUG
SPL set ID: e64c283b-0efa-0bfd-e053-2a95a90ab71d
SPL ID: 3e4fe7f8-b07f-5ac2-e063-6394a90afc08
Version: 5
Effective date: 2025-09-08
Source export date: 2026-09-28
Source partition: 2
Source file: https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:15:35

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 · 34 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M012	openfda.application_number
brand name		Medique Decorel Forte	openfda.brand_name
brand name		Medi-First Plus Cough Cold	openfda.brand_name
brand name		Medi-First Cough Cold	openfda.brand_name
generic name		ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE	openfda.generic_name
manufacturer name		Unifirst First Aid Corporation	openfda.manufacturer_name
ndc	package	47682-435-36	openfda.package_ndc
ndc	package	47682-435-80	openfda.package_ndc
ndc	package	47682-836-36	openfda.package_ndc
ndc	package	47682-836-80	openfda.package_ndc
ndc	package	47682-835-99	openfda.package_ndc
ndc	package	47682-835-36	openfda.package_ndc
ndc	package	47682-835-80	openfda.package_ndc
ndc	package	47682-836-99	openfda.package_ndc
ndc	package	47682-435-99	openfda.package_ndc
ndc	product	47682-435	openfda.product_ndc
ndc	product	47682-835	openfda.product_ndc
ndc	product	47682-836	openfda.product_ndc
ndc11	package	47682083680	derived:openfda.package_ndc
ndc11	package	47682043599	derived:openfda.package_ndc
ndc11	package	47682043536	derived:openfda.package_ndc
ndc11	package	47682083536	derived:openfda.package_ndc
ndc11	package	47682083580	derived:openfda.package_ndc
ndc11	package	47682043580	derived:openfda.package_ndc
ndc11	package	47682083636	derived:openfda.package_ndc
ndc11	package	47682083599	derived:openfda.package_ndc
ndc11	package	47682083699	derived:openfda.package_ndc
rxcui		1098435	openfda.rxcui
spl id		3e4fe7f8-b07f-5ac2-e063-6394a90afc08	id
spl set id		e64c283b-0efa-0bfd-e053-2a95a90ab71d	set_id
unii		9D2RTI9KYH	openfda.unii
unii		04JA59TNSJ	openfda.unii
unii		362O9ITL9D	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 Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take: more than 4,000 mg of acetaminophen in 24 hours with other drugs containing acetaminophen 3 or more alcoholic drinks every day while using this product Allergy alert: Acetaminophen may cause severe skin reactions. Symptoms may include: blisters rash skin reddening If a skin reaction occurs, stop use and seek medical help right away. Sore throat warning: If sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, nausea, or vomiting, consult a doctor promptly.

Reported adverse events (FAERS/openFDA)#

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