DOCTOR HOYS PAIN RELIEF GEL (menthol, camphor- synthetic gel

Doctor Hoys Pain Relief Gel by

Drug Labeling and Warnings

Doctor Hoys Pain Relief Gel by is a Otc medication manufactured, distributed, or labeled by Dynamic Blending Specialists, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

75638-010-01

75638-010-02

75638-010-03

INGREDIENTS AND APPEARANCE

DOCTOR HOYS PAIN RELIEF GEL 
menthol, camphor (synthetic) gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75638-010
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	50 mg  in 1 mL
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET)	CAMPHOR (SYNTHETIC)	50 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75638-010-00	89 mL in 1 TUBE; Type 0: Not a Combination Product	03/01/2023
2	NDC: 75638-010-01	177 mL in 1 TUBE; Type 0: Not a Combination Product	03/01/2023
3	NDC: 75638-010-02	946 mL in 1 TUBE; Type 0: Not a Combination Product	03/01/2023
4	NDC: 75638-010-03	1893 mL in 1 TUBE; Type 0: Not a Combination Product	03/01/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	03/01/2023

Labeler - Dynamic Blending Specialists, Inc. (085704438)