MUCUS RELIEF

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: MUCUS RELIEF
Generic name: GUAIFENESIN
Manufacturer: Bryant Ranch Prepack
Product type: HUMAN OTC DRUG
SPL set ID: 9ed5611f-4e1d-4f71-b430-a2a949bf7fe5
SPL ID: 752e84a6-9670-4527-aacd-4ec57bc0c3c7
Version: 8
Effective date: 2026-04-17
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 02:57:29

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 · 19 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M012	openfda.application_number
brand name		MUCUS RELIEF	openfda.brand_name
generic name		GUAIFENESIN	openfda.generic_name
manufacturer name		Bryant Ranch Prepack	openfda.manufacturer_name
ndc	package	71335-1035-3	openfda.package_ndc
ndc	package	71335-1035-4	openfda.package_ndc
ndc	package	71335-1035-1	openfda.package_ndc
ndc	package	71335-1035-5	openfda.package_ndc
ndc	package	71335-1035-2	openfda.package_ndc
ndc	product	71335-1035	openfda.product_ndc
ndc11	package	71335103502	derived:openfda.package_ndc
ndc11	package	71335103501	derived:openfda.package_ndc
ndc11	package	71335103505	derived:openfda.package_ndc
ndc11	package	71335103503	derived:openfda.package_ndc
ndc11	package	71335103504	derived:openfda.package_ndc
rxcui		359601	openfda.rxcui
spl id		752e84a6-9670-4527-aacd-4ec57bc0c3c7	id
spl set id		9ed5611f-4e1d-4f71-b430-a2a949bf7fe5	set_id
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 Ask a doctor before use if you have persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema cough accompanied by excessive phlegm (mucus) Stop use and ask a doctor if cough lasts more than 7 days or comes back cough occurs with fever, rash or persistent headache these could be signs of a serious illness. If pregnant or breast feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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