Mucosan Max with Acetaminophen

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: Mucosan Max with Acetaminophen
Generic name: ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN AND PHENYLEPHRINE HYDROCHLORIDE
Manufacturer: Menper Distributors, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 26a4861b-5d8e-9ec6-e063-6394a90af577
SPL ID: 47e2a19d-8d4b-61d1-e063-6294a90a452e
Version: 2
Effective date: 2026-01-08
Source export date: 2026-09-28
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/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:37:11

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 · 14 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M012	openfda.application_number
brand name		Mucosan Max with Acetaminophen	openfda.brand_name
generic name		ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN AND PHENYLEPHRINE HYDROCHLORIDE	openfda.generic_name
manufacturer name		Menper Distributors, Inc.	openfda.manufacturer_name
ndc	package	53145-696-06	openfda.package_ndc
ndc	product	53145-696	openfda.product_ndc
ndc11	package	53145069606	derived:openfda.package_ndc
rxcui		1116572	openfda.rxcui
spl id		47e2a19d-8d4b-61d1-e063-6294a90a452e	id
spl set id		26a4861b-5d8e-9ec6-e063-6394a90af577	set_id
unii		9D2RTI9KYH	openfda.unii
unii		04JA59TNSJ	openfda.unii
unii		362O9ITL9D	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 Liver warning: this product contains acetaminophen. Severe liver damage may occur if you take: more than 4 doses (20 mL each) in 24 hours, wich is the maximum daily amount for this product with other drugs containing acetaminophen 3 or more alcoholic drinks daily while using this product. Allergy alert: acetaminophen may cause severe skin reactions. Symptoms may include: skin reddening, blisters and rash. If skin reaction occurs, stop use and seek medical help right away. Sore throat warning: if sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, nausea or vomiting, consult a doctor promptly.

Reported adverse events (FAERS/openFDA)#

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