Menthol Drops Dollar General Severe 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 45ct
Generic name
MENTHOL
Manufacturer
Dollar General Corporation
Product type
HUMAN OTC DRUG
SPL set ID
c831d3d9-b910-40e6-bfdf-defe6850614d
SPL ID
41eb6ee3-ec97-283a-e063-6294a90ad49c
Version
2
Effective date
2025-10-24
Source export date
2026-09-28
Source partition
2
Source file
https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:14:43
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: ore 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: a severe sore throat accompanied by difficult in breathing or that lasts more than 2 days a sore 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 if 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 gelp or contact a Poison Control Center right away

Reported adverse events (FAERS/openFDA)#

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