Curewell Tussin 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: Curewell Tussin DM
Generic name: DEXTROMETHORPHAN, GUAIFENESIN
Manufacturer: RMT HEALTH LLC
Product type: HUMAN OTC DRUG
SPL set ID: 4fe9ad93-cdc4-b4df-e063-6294a90a90ae
SPL ID: 51dbb3fc-e87e-7807-e063-6394a90af808
Version: 2
Effective date: 2026-05-15
Source export date: 2026-10-27
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/2026-10-27/55ffdfed5c29f1b4aed512886bd3fb7831e157cc4948137779971a558752ed2b/drug-label-0006-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 20:07:00

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		Curewell Tussin DM	openfda.brand_name
generic name		DEXTROMETHORPHAN, GUAIFENESIN	openfda.generic_name
manufacturer name		RMT HEALTH LLC	openfda.manufacturer_name
ndc	package	85111-802-16	openfda.package_ndc
ndc	product	85111-802	openfda.product_ndc
ndc11	package	85111080216	derived:openfda.package_ndc
rxcui		996520	openfda.rxcui
spl id		51dbb3fc-e87e-7807-e063-6394a90af808	id
spl set id		4fe9ad93-cdc4-b4df-e063-6294a90a90ae	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 taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs fir depression, psychiatric or emotional conditions, or Parkinson's disease, or for 2 weeks after stopping drug contains an MAOI, as a doctor or pharmacist before taking this product.

Reported adverse events (FAERS/openFDA)#

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