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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Doctor Hoys Pain Relief Gel

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 Type HUMAN OTC DRUG Item Code (Source) NDC:10842-212
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 5.00 g  in 100 mL
CAMPHOR (NATURAL) (UNII: N20HL7Q941) (CAMPHOR (NATURAL) - UNII:N20HL7Q941) CAMPHOR (NATURAL) 5.00 g  in 100 mL
Inactive Ingredients
Ingredient Name Strength
WATER (UNII: 059QF0KO0R)  
HAMAMELIS VIRGINIANA TOP WATER (UNII: NT00Y05A2V)  
ALCOHOL (UNII: 3K9958V90M)  
GLYCERIN (UNII: PDC6A3C0OX)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)  
CANDELILLA WAX (UNII: WL0328HX19)  
HYDRATED SILICA (UNII: Y6O7T4G8P9)  
SHEA BUTTER (UNII: K49155WL9Y)  
BIOSACCHARIDE GUM-1 (UNII: BB4PU4V09H)  
OLEYL ALCOHOL (UNII: 172F2WN8DV)  
ZANTHOXYLUM BUNGEANUM FRUIT (UNII: 3CIP16A418)  
POLYSORBATE 20 (UNII: 7T1F30V5YH)  
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)  
LACTOSE (UNII: J2B2A4N98G)  
POWDERED CELLULOSE (UNII: SMD1X3XO9M)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
HYPROMELLOSES (UNII: 3NXW29V3WO)  
CHROMIUM HYDROXIDE GREEN (UNII: RV8FT8XF5R)  
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:10842-212-01 119.0 mL in 1 TUBE
2 NDC:10842-212-02 3.5 mL in 1 PACKET
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part356 07/01/2012
Labeler - DOCTOR HOY'S, LLC (791882322)

Revised: 12/2014
Document Id: 416fcb3c-3e75-423f-adaa-79ac354b735f
Set id: cb33aef3-8437-488a-a4d8-cd7bfc9043bc
Version: 8
Effective Time: 20141209
 
DOCTOR HOY'S, LLC