Guaifed 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: Guaifed DM
Generic name: DEXTROMETHORPHAN, GUAIFENESIN
Manufacturer: Aldama Pharmaceuticals, Inc
Product type: HUMAN OTC DRUG
SPL set ID: 396bf716-0f61-9563-e063-6394a90a171b
SPL ID: 58b4e715-186f-6cc6-e063-6294a90af150
Version: 6
Effective date: 2026-08-10
Source export date: 2026-09-28
Source partition: 6
Source file: https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:37:36

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 · 16 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M012	openfda.application_number
brand name		Guaifed DM	openfda.brand_name
generic name		DEXTROMETHORPHAN, GUAIFENESIN	openfda.generic_name
manufacturer name		Aldama Pharmaceuticals, Inc	openfda.manufacturer_name
ndc	package	73564-802-16	openfda.package_ndc
ndc	package	73564-802-08	openfda.package_ndc
ndc	package	73564-802-04	openfda.package_ndc
ndc	product	73564-802	openfda.product_ndc
ndc11	package	73564080208	derived:openfda.package_ndc
ndc11	package	73564080204	derived:openfda.package_ndc
ndc11	package	73564080216	derived:openfda.package_ndc
rxcui		996520	openfda.rxcui
spl id		58b4e715-186f-6cc6-e063-6294a90af150	id
spl set id		396bf716-0f61-9563-e063-6394a90a171b	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 takin a prescription monoamine oxidase inhibidor (MAOI) (certain drugs for deression, psychiatric or emotional conditions, or Parkinson's disease, or for two weeks after stoping the MAOI drug. If you do not know if nyour 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.