HEALTH MART PAIN RELIEF- camphor, menthol, and methyl salicylate patch 
McKesson

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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Active ingredients                                                       Purpose

Camphor 1.2%.........................................................Topical analgesic

Menthol 5.7%...........................................................Topical analgesic

Methyl salicylate 6.3%...............................................Topical analgesic

Uses

for temporary relief of minor aches & pains of muscles & joints associated with:

Warnings

For external use only

Allergy alert: If prone to allergic reaction from aspirin or salicylates, consult a doctor before use.

Do not use

Stop use and ask a doctor if

If pregnant or breast feeding, ask a health professional before use.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

adults and children 12 years of age and over:

children under 12 years of age:

Other information

Inactive ingredients

glyceryl hydrogenated rosinate, hydrated silica, mineral oil, polyethylene glycol 400, polyisobutylene (1300 MW), styrene/isoprene copolymer, YS resin, zinc oxide

Distributed by:

McKesson

One Post Street

San Franciso, CA 94104

www.healthmart.com/healthmartbrand

image description

HEALTH MART PAIN RELIEF 
camphor, menthol, and methyl salicylate patch
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62011-0328
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC)7.1 mg
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL33 mg
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE36 mg
Inactive Ingredients
Ingredient NameStrength
HYDRATED SILICA (UNII: Y6O7T4G8P9)  
MINERAL OIL (UNII: T5L8T28FGP)  
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
POLYISOBUTYLENE (1300 MW) (UNII: 241BN7J12Y)  
STYRENE (UNII: 44LJ2U959V)  
ISOPRENE (UNII: 0A62964IBU)  
ZINC OXIDE (UNII: SOI2LOH54Z)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:62011-0328-140 in 1 BOX; Type 0: Not a Combination Product01/23/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34801/23/2017
Labeler - McKesson (177667227)
Registrant - United Exchange Corp. (840130579)
Establishment
NameAddressID/FEIBusiness Operations
Foshan Aqua Gel Biotech Co., Ltd.529128763manufacture(62011-0328)

Revised: 1/2017
Document Id: b12015d0-6514-4f68-bebd-88ed2048821b
Set id: bff95a85-0f98-4a55-8241-f2bb37256724
Version: 1
Effective Time: 20170123
 
McKesson