Tukol MAX ACTION Severe Congestion and 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: Tukol MAX ACTION Severe Congestion and Cough
Generic name: DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL
Manufacturer: Genomma Lab USA, Inc
Product type: HUMAN OTC DRUG
SPL set ID: 9ac3e24a-d18a-48fc-8005-55393085d57b
SPL ID: 249ec14a-4df6-4fa2-e063-6294a90ad340
Version: 8
Effective date: 2024-10-16
Source export date: 2026-09-28
Source partition: 7
Source file: https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:44:44

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 · 13 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M012	openfda.application_number
brand name		Tukol MAX ACTION Severe Congestion and Cough	openfda.brand_name
generic name		DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL	openfda.generic_name
manufacturer name		Genomma Lab USA, Inc	openfda.manufacturer_name
ndc	package	50066-517-25	openfda.package_ndc
ndc	product	50066-517	openfda.product_ndc
ndc11	package	50066051725	derived:openfda.package_ndc
rxcui		1043543	openfda.rxcui
spl id		249ec14a-4df6-4fa2-e063-6294a90ad340	id
spl set id		9ac3e24a-d18a-48fc-8005-55393085d57b	set_id
unii		9D2RTI9KYH	openfda.unii
unii		04JA59TNSJ	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, psychiatic, or emotional conditions, or Parkinson's disease), or for 2 weeks after stopping an 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.