Dextromethorphan HBr and Guaifenesin Oral Solution

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: Dextromethorphan HBr and Guaifenesin Oral Solution
Generic name: DEXTROMETHORPHAN HBR AND GUAIFENESIN ORAL SOLUTION
Manufacturer: KESIN PHARMA CORPORATION
Product type: HUMAN OTC DRUG
SPL set ID: 284eae44-81bc-400c-e063-6394a90af446
SPL ID: 2cee75e1-ee97-6129-e063-6394a90a03dd
Version: 3
Effective date: 2025-01-30
Source export date: 2026-10-27
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/2eee27992d1f29d82f827fd5be42f1314ed39ce4c497af5d81435ac6656a0957/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 20:24:53

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 · 18 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M012	openfda.application_number
brand name		Dextromethorphan HBr and Guaifenesin Oral Solution	openfda.brand_name
generic name		DEXTROMETHORPHAN HBR AND GUAIFENESIN ORAL SOLUTION	openfda.generic_name
manufacturer name		KESIN PHARMA CORPORATION	openfda.manufacturer_name
ndc	package	81033-103-50	openfda.package_ndc
ndc	package	81033-103-51	openfda.package_ndc
ndc	package	81033-103-10	openfda.package_ndc
ndc	package	81033-103-05	openfda.package_ndc
ndc	product	81033-103	openfda.product_ndc
ndc11	package	81033010351	derived:openfda.package_ndc
ndc11	package	81033010310	derived:openfda.package_ndc
ndc11	package	81033010350	derived:openfda.package_ndc
ndc11	package	81033010305	derived:openfda.package_ndc
rxcui		996520	openfda.rxcui
spl id		2cee75e1-ee97-6129-e063-6394a90a03dd	id
spl set id		284eae44-81bc-400c-e063-6394a90af446	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 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.