THROATCALM

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: THROATCALM
Generic name: ECHINACEA ANGUSTIFOLIA WHOLE, PLANTAGO MAJOR WHOLE
Manufacturer: Boiron
Product type: HUMAN OTC DRUG
SPL set ID: f5788da2-f60b-d0b8-e053-2995a90a11c7
SPL ID: 29904ee4-5ece-e1b7-e063-6294a90aba32
Version: 3
Effective date: 2024-12-18
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 21:01:38

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 · 10 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		THROATCALM	openfda.brand_name
generic name		ECHINACEA ANGUSTIFOLIA WHOLE, PLANTAGO MAJOR WHOLE	openfda.generic_name
manufacturer name		Boiron	openfda.manufacturer_name
ndc	package	0220-9329-77	openfda.package_ndc
ndc	product	0220-9329	openfda.product_ndc
ndc11	package	00220932977	derived:openfda.package_ndc
spl id		29904ee4-5ece-e1b7-e063-6294a90aba32	id
spl set id		f5788da2-f60b-d0b8-e053-2995a90a11c7	set_id
unii		W2469WNO6U	openfda.unii
unii		VB06AV5US8	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

Sore Throat Warning: Severe or persistent throat or sore throat accompanied by high fever, headache, nausea, and vomiting may be serious. Consult a doctor promptly. Do not use more than 2 days or administer to children under 12 years of age unless directed by a doctor.

Reported adverse events (FAERS/openFDA)#

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