LEADER MEDICATED RELIEF PATCH- camphor (synthetic) levomenthol salicylic acid patch 
CARDINAL HEALTH, INC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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LEADER Relief Patch No-Mess Topical Analgesic

ACTIVE INGREDIENT

Active IngredientPurpose
 DL-Camphor 1.2% Topical Analgesic
 L-Menthol 5.7% Topical Analgesic
 Methyl Salicylate 6.3% Topical Analgesic

INACTIVE INGREDIENT

Glyceryl Hydrogenated Rosinate, Styrene/Isoprene Copolymer, Hydrated Silica, Mineral Oil, Polyisobutylene (1300 MW), PEG-400, Zinc Oxide, Ys Resin.

KEEP OUT OF REACH OF CHILDREN

If swallowed, get medical help or contact a Poison Control Center right away.

INDICATIONS & USAGE

Temporary relief of aches and pains associated with arthritis, simple backache, strains, sprains, bruises.

WARNINGS

For External Use Only

DOSAGE & ADMINISTRATION

Adults and children over 12 years: clean and dry affected area. Carefully remove backing from patch. Apply sticky side of patch to affected area.

Wear one patch up to 8 hours. Repeat as necessary, no more than 4 times daily, no more than 7 consecutive days.

Children 12 years or younger, consult a physician.

PURPOSE

Topical Analgesic

When using this product:

Do not use

top use and consult a doctor

Storage and Care

Store in a clean, dry place outside of direct sunlight. Protect from excessive moisture.

Medicated Relief

Label Image
LEADER MEDICATED RELIEF PATCH 
camphor (synthetic) levomenthol salicylic acid patch
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70000-0206
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC)1.2 
LEVOMENTHOL (UNII: BZ1R15MTK7) (LEVOMENTHOL - UNII:BZ1R15MTK7) LEVOMENTHOL5.7 
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE6.3 
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
STYRENE (UNII: 44LJ2U959V)  
HYDRATED SILICA (UNII: Y6O7T4G8P9)  
MINERAL OIL (UNII: T5L8T28FGP)  
POLYISOBUTYLENE (1100000 MW) (UNII: FLT10CH37X)  
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
ZINC OXIDE (UNII: SOI2LOH54Z)  
NATURAL LATEX RUBBER (UNII: 2LQ0UUW8IN)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70000-0206-120 in 1 BOX12/01/2016
11 in 1 POUCH; Type 0: Not a Combination Product
2NDC:70000-0206-240 in 1 BOX12/01/2016
21 in 1 POUCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34812/01/2016
Labeler - CARDINAL HEALTH, INC (063997360)
Establishment
NameAddressID/FEIBusiness Operations
Foshan Aqua Gel Biotech Co., Ltd.,529128763manufacture(70000-0206)

Revised: 1/2022
Document Id: d4efd80c-ce47-4b6f-e053-2a95a90a27d8
Set id: 80f68cdf-9601-495f-a7cb-fd9bdb35fde6
Version: 3
Effective Time: 20220106
 
CARDINAL HEALTH, INC