Sore Throat

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
Sore Throat
Generic name
TEUCRIUM SCORODONIA, VERONICA OFFICINALIS, EQUISETUM HYEMALE, FUMARIA OFFICINALIS, GERANIUM ROBERTIANUM, NASTURTIUM AQUATICUM, NATRUM SULPHURICUM, PINUS SYLVESTRIS, GENTIANA LUTEA, SARSAPARILLA (SMILAX REGELII), SCROPHULARIA NODOSA, MYOSOTIS ARVENSIS, ARANEA DIADEMA, JUGLANS REGIA, CALCAREA PHOSPHORICA, FERRUM IODATUM, LYMPH NODE (SUIS), THYROIDINUM (SUIS)
Manufacturer
Deseret Biologicals, Inc.
Product type
HUMAN OTC DRUG
SPL set ID
3d09dd25-5310-4ed5-9512-a160531425f3
SPL ID
5e5ed349-f84a-4be8-b9bb-5f42ac806977
Version
4
Effective date
2024-04-02
Source export date
2026-10-12
Source partition
11
Source file
https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/a497e765d824a2e2aa9e88d5f0eea2aae9dcba363989e5f163395cda5c3c9dd8/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:44:41
Harmonized routes table
Harmonized routes
ORAL

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: If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away. Severe or persistent sore throat or sore throat accompanied by high fever, headache, nausea, and vomiting may be serious. Consult a physician promptly. Do not use more than two days or administer to children under 3 years of age unless directed by a physician. Tamper Evident: Sealed for your protection. Do not use if seal is broken or missing.

Reported adverse events (FAERS/openFDA)#

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