Leader Ice Blue Analgesic

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: Leader Ice Blue Analgesic
Generic name: MENTHOL, UNSPECIFIED FORM
Manufacturer: Cardinal Health, 110 dba LEADER
Product type: HUMAN OTC DRUG
SPL set ID: 952e56ea-5cbc-4078-bd01-5d3b6864a5ce
SPL ID: d75b3f1d-de2b-4e0c-bb0e-fa668d384046
Version: 4
Effective date: 2024-02-09
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 05:25:29

Harmonized routes table
Harmonized routes
TOPICAL

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		M017	openfda.application_number
brand name		Leader Ice Blue Analgesic	openfda.brand_name
generic name		MENTHOL, UNSPECIFIED FORM	openfda.generic_name
manufacturer name		Cardinal Health, 110 dba LEADER	openfda.manufacturer_name
ndc	package	70000-0260-1	openfda.package_ndc
ndc	product	70000-0260	openfda.product_ndc
ndc11	package	70000026001	derived:openfda.package_ndc
rxcui		311502	openfda.rxcui
spl id		d75b3f1d-de2b-4e0c-bb0e-fa668d384046	id
spl set id		952e56ea-5cbc-4078-bd01-5d3b6864a5ce	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 For external use only Do not use do not use with other topical pain relievers do not use with heating pads or other heating devices When using this product avoid contact with the eyes do not bandage tightly do not apply to wounds or damaged skin Stop use and consult a doctor if condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days. If pregnant or breastfeeding, ask a health professional before use Keep out of reach of children . If swallowed, get medical help or contact a Poison Control Center immediately at 1-800-222-1222.

Reported adverse events (FAERS/openFDA)#

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