Tusnel Diabetic

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: Tusnel Diabetic
Generic name: DEXTROMETHORPHAN, GUAIFENESIN
Manufacturer: LLORENS PHARMACEUTICALS INTERNATIONAL DIVISION
Product type: HUMAN OTC DRUG
SPL set ID: 66b3c094-809e-4d2c-bc15-46563de685cb
SPL ID: 471f18f8-553e-41f9-e063-6394a90ae51e
Version: 7
Effective date: 2025-12-29
Source export date: 2026-11-06
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/97001096994db9ca8cee114e6c3bb5298d3c573158ffc1ab8692d82e76a3eb40/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 06:55:30

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		Tusnel Diabetic	openfda.brand_name
generic name		DEXTROMETHORPHAN, GUAIFENESIN	openfda.generic_name
manufacturer name		LLORENS PHARMACEUTICALS INTERNATIONAL DIVISION	openfda.manufacturer_name
ndc	package	54859-505-16	openfda.package_ndc
ndc	package	54859-505-04	openfda.package_ndc
ndc	product	54859-505	openfda.product_ndc
ndc11	package	54859050504	derived:openfda.package_ndc
ndc11	package	54859050516	derived:openfda.package_ndc
rxcui		996520	openfda.rxcui
spl id		471f18f8-553e-41f9-e063-6394a90ae51e	id
spl set id		66b3c094-809e-4d2c-bc15-46563de685cb	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 inhibitor (MAOI) (certain drugs for depression, psychiatric, or emotional conditions, or Parkinson's disease), or if 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 giving this product.

Reported adverse events (FAERS/openFDA)#

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