DOCTOR HOYS NATURAL PAIN RELIEF- menthol and camphor (natural) gel 
DOCTOR HOY'S, LLC

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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DRUG FACTS

ACTIVE INGREDIENTS:          
CAMPHOR (5%)                       

MENTHOL (5%)                        

Purpose

TOPICAL ANALGESIC

USES:

TEMPORARY RELIEF OF MINOR ACHES AND PAINS OF MUSCLES AND JOINTS DUE TO

WARNINGS

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DIRECTIONS

INACTIVE INGREDIENTS

ARNICA MONTANA FLOWER EXTRACT, HAMAMELIS VIRGINIANA (WITCH HAZEL) WATER,  WATER, AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER, BIOSACCHARIDE GUM-1, BUTYROSPERMUM PARKII (SHEA BUTTER) FRUIT,  CELLULOSE, ALCOHOL, ETHYLHEXYLGLYCERIN, EUPHORBIA CERIFERA (CANDELILLA) WAX, GLYCERIN, HYDROLYZED SILICA, HYDROXYPROPYL METHYLCELLULOSE, LACTOSE, PHENOXYETHANOL, OLEYL ALCOHOL, POLYSORBATE 20, SD ALCOHOL 40-B, SODIUM STARCH OCTNYLSUCCINATE, TOCOPHERYL ACETATE, ZANTHOXYLUM BUNGEANUM FRUIT EXTRACT, CHROMIUM HYDROXIDE GREEN

Distributed by : DOCTOR HOY'S, LLC MESA, AZ 85209

(866) 674-8000   www.drhoys.com

DrHoysPainGel

DOCTOR HOYS NATURAL PAIN RELIEF 
camphor menthol gel
Product Information
Product TypeHUMAN OTC DRUG LABELItem Code (Source)NDC:10842-212
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (MENTHOL) MENTHOL5.00 g  in 100 mL
CAMPHOR (NATURAL) (CAMPHOR (NATURAL)) CAMPHOR (NATURAL)5.00 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
HAMAMELIS VIRGINIANA TOP WATER 
ALCOHOL 
GLYCERIN 
PHENOXYETHANOL 
ETHYLHEXYLGLYCERIN 
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER 
CANDELILLA WAX 
HYDRATED SILICA 
SHEA BUTTER 
BIOSACCHARIDE GUM-1 
OLEYL ALCOHOL 
ZANTHOXYLUM BUNGEANUM FRUIT 
POLYSORBATE 20 
ARNICA MONTANA FLOWER 
LACTOSE 
POWDERED CELLULOSE 
.ALPHA.-TOCOPHEROL ACETATE 
HYPROMELLOSES 
CHROMIUM HYDROXIDE GREEN 
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:10842-212-01119.0 mL in 1 TUBE
2NDC:10842-212-023.5 mL in 1 PACKET
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35607/01/2012
Labeler - DOCTOR HOY'S, LLC (791882322)

Revised: 6/2014
Document Id: 6932adc2-af2b-4aef-a30b-2e147c80e1ce
Set id: cb33aef3-8437-488a-a4d8-cd7bfc9043bc
Version: 6
Effective Time: 20140609
 
DOCTOR HOY'S, LLC