DOCTOR HOYS PAIN RELIEF GEL- menthol, camphor (synthetic) gel 
Dynamic Blending Specialists, Inc.

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Doctor Hoy's Pain Relief Gel

Drug Facts:

Active ingredients:

Menthol (5%)

Camphor (5%)

Purpose:

Topical Analgesic

Uses:

Temporary relief of minor aches and pains of muscles and joints due to: simple backache • arthritis • sprains • strains 

Warnings:

• For external use only

• Use as directed 

• Avoid contact with eyes or mucus membranes

• Do not apply to open wounds, irritated or damaged skin

Keep Out of reach of children

If swallowed, get medical help or contact a Poison Control Center immediately 

If pregnant or breast feeding,

• ask a health professional before use

• Discontinue use of this product and consult a physician if condition worsens, or if symptoms persist for more than 7 days, or clear up and occur again within a few days 

• Use caution with wrap or heating pad.

Directions:

For adults and children 2 years and older: For best results, shake well and apply generously. Use 1 layer for minor pain, 2 layers for medium and 3 layers for severe symptoms • Rub in well and allow to dry between layers (usually 2-3 minutes) • Repeat process up to 4 times daily • for children under 2 years of age: Consult a physician before use.

Inactive ingedients:

Alcohol, Ammonium Acryloyldimethyltaurate/VP Copolymer, Arnica Montana (Arnica Flower) Extract, Biosaccharide Gum-1, Butyrospermum Parkii (Shea) Butter Extract, Ethylhexylglycerin, Euphorbia Cerifera (Candelilla) Wax, Glycerin, Hamamelis Virginiana (Witch Hazel) Water, Hydrated Silica, Jojoba Esters, Phenoxyethanol, Polyglyceryl-10 Caprylate/Caprate, SD Alcohol 40-B, Sodium Starch Octenylsuccinate, Tocopherol Acetate, Water, Zanthoxylum Bungeanum Fruit Extract.

75638-010-00

Label89ml

75638-010-01

Label177ml

75638-010-02

Label946ml

75638-010-03

Label1893ml

DOCTOR HOYS PAIN RELIEF GEL 
menthol, camphor (synthetic) gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75638-010
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL50 mg  in 1 mL
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC)50 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)  
ARNICA MONTANA WHOLE (UNII: O80TY208ZW)  
BIOSACCHARIDE GUM-1 (UNII: BB4PU4V09H)  
SHEA BUTTER (UNII: K49155WL9Y)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
CANDELILLA WAX (UNII: WL0328HX19)  
GLYCERIN (UNII: PDC6A3C0OX)  
HAMAMELIS VIRGINIANA TOP WATER (UNII: NT00Y05A2V)  
HYDRATED SILICA (UNII: Y6O7T4G8P9)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
WATER (UNII: 059QF0KO0R)  
ZANTHOXYLUM BUNGEANUM FRUIT (UNII: 3CIP16A418)  
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:75638-010-0089 mL in 1 TUBE; Type 0: Not a Combination Product03/01/2023
2NDC:75638-010-01177 mL in 1 TUBE; Type 0: Not a Combination Product03/01/2023
3NDC:75638-010-02946 mL in 1 TUBE; Type 0: Not a Combination Product03/01/2023
4NDC:75638-010-031893 mL in 1 TUBE; Type 0: Not a Combination Product03/01/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01703/01/2023
Labeler - Dynamic Blending Specialists, Inc. (085704438)

Revised: 12/2023
Document Id: 0d0d2163-f953-ccff-e063-6394a90a5d60
Set id: 50123bb9-d5d8-4ba6-ab94-8ed95fe0f5a8
Version: 2
Effective Time: 20231221
 
Dynamic Blending Specialists, Inc.