Curist Mucus Relief Maximum Strength

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: Curist Mucus Relief Maximum Strength
Generic name: GUAIFENESIN
Manufacturer: Little Pharma, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: c7d1136c-a712-2ac5-e053-2995a90a4dd4
SPL ID: 59d14f50-a21c-58ca-e063-6394a90a1e8a
Version: 10
Effective date: 2026-08-24
Source export date: 2026-10-27
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/2026-10-27/977776a6cc37ec1c77259da8a93ae161850a3aa120341096e5a03428b84d016b/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 21:00:25

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 · 20 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application applno	ANDA	213420	derived:openfda.application_number
application number		ANDA213420	openfda.application_number
brand name		Curist Mucus Relief Maximum Strength	openfda.brand_name
generic name		GUAIFENESIN	openfda.generic_name
manufacturer name		Little Pharma, Inc.	openfda.manufacturer_name
ndc	package	72559-013-11	openfda.package_ndc
ndc	package	72559-013-28	openfda.package_ndc
ndc	package	72559-013-41	openfda.package_ndc
ndc	package	72559-013-23	openfda.package_ndc
ndc	package	72559-013-64	openfda.package_ndc
ndc	product	72559-013	openfda.product_ndc
ndc11	package	72559001341	derived:openfda.package_ndc
ndc11	package	72559001323	derived:openfda.package_ndc
ndc11	package	72559001364	derived:openfda.package_ndc
ndc11	package	72559001311	derived:openfda.package_ndc
ndc11	package	72559001328	derived:openfda.package_ndc
rxcui		310621	openfda.rxcui
spl id		59d14f50-a21c-58ca-e063-6394a90a1e8a	id
spl set id		c7d1136c-a712-2ac5-e053-2995a90a4dd4	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 Do not use for children under 12 years of age 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 too much phlegm (mucus) Stop use and ask a doctor if cough lasts more than 7 days, comes back, or 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.

Reported adverse events (FAERS/openFDA)#

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