FDA.reportPublic FDA data

Curewell Tussin DM

openFDA label record#

Cross-check layer: This is openFDA JSON-derived label data. Use the corresponding DailyMed SPL as the canonical 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
2026-08-01
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/2026-08-01/4d7120b2932458966cd5c2f0e3ab49319f616f09498d059c9ff283a8dac64565/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:11:01
Harmonized routes table
Harmonized routes
ORAL

Warnings cross-check#

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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.