Giltuss Honey DM Cough

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: Giltuss Honey DM Cough
Generic name: DEXTROMETHORPHAN HBR
Manufacturer: Dextrum Laboratories, Inc
Product type: HUMAN OTC DRUG
SPL set ID: 3f79137f-f0b0-d22c-e063-6394a90a7245
SPL ID: 3f79137f-f0b1-d22c-e063-6394a90a7245
Version: 1
Effective date: 2025-09-23
Source export date: 2026-10-12
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/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:12:20

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 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M012	openfda.application_number
brand name		Giltuss Honey DM Cough	openfda.brand_name
generic name		DEXTROMETHORPHAN HBR	openfda.generic_name
manufacturer name		Dextrum Laboratories, Inc	openfda.manufacturer_name
ndc	package	65852-004-04	openfda.package_ndc
ndc	product	65852-004	openfda.product_ndc
ndc11	package	65852000404	derived:openfda.package_ndc
rxcui		1090496	openfda.rxcui
spl id		3f79137f-f0b1-d22c-e063-6394a90a7245	id
spl set id		3f79137f-f0b0-d22c-e063-6394a90a7245	set_id
unii		9D2RTI9KYH	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

Warning Warnings Do not use If you are taking a prescription monoamine oxidase inhibitor (MAOI) ( certains drugs for depression, psychiatric, or emotional conditions, or Parkinson's disease), or for 2 weeks after stopping the MAOI drug. If you dont know is your prescription drug contains and MAOI, ask a doctor or pharmacist before taking this product. Warnings

Reported adverse events (FAERS/openFDA)#

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