Leader Ultra Strength Muscle Rub Topical 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 Ultra Strength Muscle Rub Topical Analgesic
Generic name: CAMPHOR (SYNTHETIC), MENTHOL, UNSPECIFIED FORM, AND METHYL SALICYLATE
Manufacturer: Cardinal Health, 110 dba LEADER
Product type: HUMAN OTC DRUG
SPL set ID: 9d99a900-60e0-454c-98e0-2c63eb910cf1
SPL ID: e3f093f8-52f5-4130-a42b-8b3c8eb2a138
Version: 5
Effective date: 2024-02-09
Source export date: 2026-10-12
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/2026-10-12/4760f38f2bcb10aa20ddbadb42b270d31e9f2a8024440d3af3dec8d11feb92ec/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:27:32

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 · 15 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		Leader Ultra Strength Muscle Rub Topical Analgesic	openfda.brand_name
generic name		CAMPHOR (SYNTHETIC), MENTHOL, UNSPECIFIED FORM, AND METHYL SALICYLATE	openfda.generic_name
manufacturer name		Cardinal Health, 110 dba LEADER	openfda.manufacturer_name
ndc	package	70000-0208-1	openfda.package_ndc
ndc	package	70000-0208-2	openfda.package_ndc
ndc	product	70000-0208	openfda.product_ndc
ndc11	package	70000020801	derived:openfda.package_ndc
ndc11	package	70000020802	derived:openfda.package_ndc
rxcui		283083	openfda.rxcui
spl id		e3f093f8-52f5-4130-a42b-8b3c8eb2a138	id
spl set id		9d99a900-60e0-454c-98e0-2c63eb910cf1	set_id
unii		L7T10EIP3A	openfda.unii
unii		5TJD82A1ET	openfda.unii
unii		LAV5U5022Y	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 with a heating pad on wounds, damaged, broken or irritated skin on a child under 12 years of age with arthritis-like conditions Ask a doctor before use if you have redness over the affected area When using this product use only as directed do not swallow do not bandage tightly avoid contact with the eyes and mucous membranes Stop use and consult a doctor if skin redness or irritation develops condition worsens or pain lasts for more than 7 days symptoms clear up and occur again within a few days Keep out of reach of children . If swallowed, 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.