Menthol Drops Dollar General Severe Honey Lemon 45ct

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
Menthol Drops Dollar General Severe Honey Lemon 45ct
Generic name
MENTHOL
Manufacturer
Dollar General Corporation
Product type
HUMAN OTC DRUG
SPL set ID
0ea61a4c-690a-4349-9952-cc17fb1f0671
SPL ID
40ab20f0-2291-f128-e063-6394a90a9ead
Version
4
Effective date
2025-10-08
Source export date
2026-10-12
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:12:08
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 Sore throat warning: severe or persistent sore throat or sore throat accompanied by high fever, headache, nausea and vomiting may be serious. Consult doctor promptly. Do not use more than 2 days or administer to children under 12 years of age. Ask a doctor before use if you have: severe sore throat accompanied by difficult in breathing or that lasts more than 2 days. sore throat accompanied by fever, headache, rash, swelling, nausea or vomiting Stop use and ask a doctor if sore mouth symptoms do not improve in 7 days, or irritation, pain or redness lasts or worsens. 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.