Revasol Tussin DM Max with Honey

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: Revasol Tussin DM Max with Honey
Generic name: DEXTROMETHORPHAN HBR AND GUAIFENESIN
Manufacturer: Rnv LLC
Product type: HUMAN OTC DRUG
SPL set ID: 30da9255-c93a-84d6-e063-6394a90a7c2a
SPL ID: 30da9255-c93b-84d6-e063-6394a90a7c2a
Version: 1
Effective date: 2025-03-21
Source export date: 2026-10-30
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-30/a3e33fe073aa0aa94eb690c6684c74434c63cebfbf7c5530205a2c3e957ecb8b/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run: 20261102T182004Z
Imported at: 2026-11-02 19:44:11

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 · 12 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M012	openfda.application_number
brand name		Revasol Tussin DM Max with Honey	openfda.brand_name
generic name		DEXTROMETHORPHAN HBR AND GUAIFENESIN	openfda.generic_name
manufacturer name		Rnv LLC	openfda.manufacturer_name
ndc	package	84379-274-04	openfda.package_ndc
ndc	product	84379-274	openfda.product_ndc
ndc11	package	84379027404	derived:openfda.package_ndc
rxcui		2692303	openfda.rxcui
spl id		30da9255-c93b-84d6-e063-6394a90a7c2a	id
spl set id		30da9255-c93a-84d6-e063-6394a90a7c2a	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 wekks 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.