Severe Throat Sore Drops

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: Severe Throat Sore Drops
Generic name: MENTHOL
Manufacturer: Target Corporation Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 949543d5-5043-ac06-e053-2995a90ab398
SPL ID: 23e54a26-5a82-2024-e063-6294a90a2aa3
Version: 3
Effective date: 2024-10-07
Source export date: 2026-10-12
Source partition: 7
Source file: https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/ff22b88bd32e56cbc369af80345075227138a42b1b3ba9a84f038fd5493a7a47/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:55:29

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 · 10 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M012	openfda.application_number
brand name		Severe Throat Sore Drops	openfda.brand_name
generic name		MENTHOL	openfda.generic_name
manufacturer name		Target Corporation Inc.	openfda.manufacturer_name
ndc	package	11673-143-01	openfda.package_ndc
ndc	product	11673-143	openfda.product_ndc
ndc11	package	11673014301	derived:openfda.package_ndc
spl id		23e54a26-5a82-2024-e063-6294a90a2aa3	id
spl set id		949543d5-5043-ac06-e053-2995a90ab398	set_id
unii		L7T10EIP3A	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 Sore throat warning: severe or persistence sore throat accompanied or followed 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.

Reported adverse events (FAERS/openFDA)#

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