Leader Ultra Strength Muscle Rub

Manufacturer
Cardinal Health, Inc.
Effective date
2017-08-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:12:44

Label at a glance#

ProductLeader Ultra Strength Muscle Rub
Active ingredientCAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATE
Label structure13 sections

Storage and handling

Other information store between 20° to 25°C (68° to 77°F) lot no. & exp. date: see carton or see crimp of tube

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients                                 Purpose

Camphor 4%...................................Topical analgesic

Menthol 10%...................................Topical analgesic

Methyl salicylate 30%.......................Topical analgesic

OTC - PURPOSE SECTION

Uses temporarily relieves the minor aches and pains of muscles and joints associated with:

  • simple backache
  • arthritis
  • strains
  • bruises
  • sprains

WARNINGS SECTION

Warnings

For external use only

OTC - DO NOT USE SECTION

Do not use

  • on wounds or damaged skin
  • with a heating pad
  • on a child under 12 years of age with arthritis-like conditions

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you

  • have a redness over the affected area

OTC - WHEN USING SECTION

When using this product

  • avoid contact with eyes or mucous membranes
  • do not bandage tightly

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • condition worsens or symptoms persist for more than 7 days
  • symptoms clear up and occur again within a few days
  • excessive skin irritation occurs

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children to avoid accidental ingestion.

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

INDICATIONS & USAGE SECTION

Directions

  • use only as directed
  • adults and children 12 years of age and older: apply to affected area not more than 3 to 4 times daily
  • children under 12 years of age: ask a doctor

STORAGE AND HANDLING SECTION

Other information

  • store between 20° to 25°C (68° to 77°F)
  • lot no. & exp. date: see carton or see crimp of tube

INACTIVE INGREDIENT SECTION

Inactive ingredients

glycerin, isopropyl myristate, lanolin, methylparaben, petrolatum, polysorbate 60, potassium cetyl phosphate, propylparaben, sorbitan monostearate, stearyl alcohol, water

DOSAGE & ADMINISTRATION SECTION

DISTRIBUTED BY

CARDINAL HEALTH

DUBLIN, OHIO 43017

www.myleader.com

1-800-200-6313

Essential to care™since 1979

Made in Korea

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70000-0238-12025-09-22C16284748780-1d6a99b39-d01e-a426-e053-dadaa90af4c2439e9c9c-ccb8-4e33-bee3-6a441e99f629
70000-0238-12022-01-28C16284748780-1d6a99b39-d01e-a426-e053-dadaa90af4c2439e9c9c-ccb8-4e33-bee3-6a441e99f629

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70000-0238LEADER ULTRA STRENGTH MUSCLE RUB (CAMPHOR, MENTHOL, AND METHYL SALICYLATE) CREAM [CARDINAL HEALTH, INC.]1Legacy NDC20170822_439e9c9c-ccb8-4e33-bee3-6a441e99f629.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
70000-0238-1GM - Gram70000-02386f7b8bcb-81ad-457e-adc2-3498deeda39b12018-03-08

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70000-023870000-0238-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
04a26fb9-7f66-43eb-b270-79391c568705439e9c9c-ccb8-4e33-bee3-6a441e99f6292025-09-12WarningsExact identifier
spl set id: 439e9c9c-ccb8-4e33-bee3-6a441e99f629

Reported adverse events (FAERS/openFDA)#

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