Lemon Mint 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: Lemon Mint Drops
Generic name: MENTHOL
Manufacturer: Target Corporation Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 1876df19-398a-23d8-e063-6394a90ae7e8
SPL ID: 1876c89e-a7ca-c361-e063-6294a90a070c
Version: 1
Effective date: 2024-05-14
Source export date: 2026-09-28
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:24:08

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 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M012	openfda.application_number
brand name		Lemon Mint Drops	openfda.brand_name
generic name		MENTHOL	openfda.generic_name
manufacturer name		Target Corporation Inc.	openfda.manufacturer_name
ndc	package	82442-202-01	openfda.package_ndc
ndc	product	82442-202	openfda.product_ndc
ndc11	package	82442020201	derived:openfda.package_ndc
rxcui		701201	openfda.rxcui
spl id		1876c89e-a7ca-c361-e063-6294a90a070c	id
spl set id		1876df19-398a-23d8-e063-6394a90ae7e8	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: if sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash swelling, nausea or vomiting , consult a doctor promptly. If sore mouth symptons do not improve in 7 days, see your dentist or doctor promptly. These symptons may be serious .

Reported adverse events (FAERS/openFDA)#

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