BRONCOCHEM MAXIMUM COUGH KIDS

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: BRONCOCHEM MAXIMUM COUGH KIDS
Generic name: DEXTROMETHORPHAN HBR-GUAIFENESIN
Manufacturer: LABORATORIO MAGNACHEM INTERNATIONAL SRL
Product type: HUMAN OTC DRUG
SPL set ID: b0fd2f2f-5cc4-4813-8f99-c78fbe898656
SPL ID: c63d515a-0755-4d0e-8aba-aca050df0456
Version: 4
Effective date: 2025-03-13
Source export date: 2026-10-12
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/2026-10-12/edd23646015c9adc800cdbe2b778398a2d2b70e90dce5721ef2b191499a0397f/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:53:35

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		M	openfda.application_number
brand name		BRONCOCHEM MAXIMUM COUGH KIDS	openfda.brand_name
generic name		DEXTROMETHORPHAN HBR-GUAIFENESIN	openfda.generic_name
manufacturer name		LABORATORIO MAGNACHEM INTERNATIONAL SRL	openfda.manufacturer_name
ndc	package	65131-180-98	openfda.package_ndc
ndc	product	65131-180	openfda.product_ndc
ndc11	package	65131018098	derived:openfda.package_ndc
rxcui		1298228	openfda.rxcui
spl id		c63d515a-0755-4d0e-8aba-aca050df0456	id
spl set id		b0fd2f2f-5cc4-4813-8f99-c78fbe898656	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) or two weeks after stopping the MAOI drug (certain drugs for depression, psychiatric or emotional conditions may contain MAOI), if you are uncertain whether your prescription contains 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.