DOCTOR HOYS NATURAL PAIN RELIEF- camphor, menthol gel

Doctor Hoys Natural Pain Relief by

Drug Labeling and Warnings

Doctor Hoys Natural Pain Relief by is a Otc medication manufactured, distributed, or labeled by DOCTOR HOY'S, LLC, Specialty Formulations and Manufacturing LLC, Dynamic Blending Specialists, Inc., United Laboratories Manufacturing, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredients      Purpose

Camphor (5%)          External Analgesic        
Menthol (5%)          External Analgesic

PURPOSE

Uses:
for the temporary relief of minor aches and pains of muscles and joints due to:
* simple backache * arthritis * sprains * strains * bruises

KEEP OUT OF REACH OF CHILDREN

Warnings:
* for external use only * do not apply to wounds or damaged skin or bandage tightly * avoid contact with eyes * Keep out of reach of children. if swallowed, get medical help or contact a Poison Control Center immediately * if condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a physician * Pregnancy-breast feeding warning: if pregnant or breast feeding, ask a health professional before use * do not bandage tightly

INACTIVE INGREDIENT

Inactive Ingredients:

distilled water, hamamelis virginiana (witch hazel extract),
isopropyl alcohol, arnica Montana, oleyl alcohol and
zanthoxylum alatum (scezhuan pepper), Bio-saccharide
Gum -1, glycerin, ammonium acryloyldimethyltaurate/VP
copolymer, beta cyclodextrin, menthol, potassium hydroxide,
mannitol, cellulose chromium, hydroxide green, tocopheryl
acetate (vitamin E), hydroxypropyl methycellulose

DOSAGE & ADMINISTRATION

Directions:
for adults and children 2 years and older; apply to affected area not more than 3 to 4 times daily. "Children under 2 years of age: consult a doctor." Apply generously to affected and surrounding areas. Rub in well. Use 1 application for minor pain, 2 for medium and 3 applications for severs symptoms. Allow to dry between applications (usually just 2-3 minutes).

INDICATIONS & USAGE

Directions:

for adults and children 2 years and older; apply to affected area not more than 3 to 4 times daily. "Children under 2 years of age: consult a doctor."  Apply generously to affected and surrounding areas.  Rub in well. Use 1 application for minor pain, 2 for medium and 3 applications for severs symptoms.  Allow to dry between applications (usually just 2-3 minutes).

Uses:

for the temporary relief of minor aches and pains of muscles
and joints due to:

    * simple backache
    * arthritis
    * sprains
    * strains
    * bruises

WARNINGS

Warnings:

    * for external use only
    * do not apply to wounds or damaged skin or bandage tightly
    * avoid contact with eyes
    * Keep out of reach of children. if swallowed, get medical help or contact a Poison Control Center immediately
    * if condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a physician
    * Pregnancy-breast feeding warning: if pregnant or breast feeding, ask a health professional before use
    * do not bandage tightly

PRINCIPAL DISPLAY PANEL

An image/jpeg of the container label is included in this section.

 ID: MM1

INGREDIENTS AND APPEARANCE

DOCTOR HOYS NATURAL PAIN RELIEF 
camphor, menthol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10842-102
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 (NATURAL) (UNII: N20HL7Q941) (CAMPHOR (NATURAL) - UNII:N20HL7Q941)	CAMPHOR (NATURAL)	50 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ARNICA MONTANA (UNII: O80TY208ZW)
WATER (UNII: 059QF0KO0R)
WITCH HAZEL (UNII: 101I4J0U34)
ISOPROPYL ALCOHOL (UNII: ND2M416302)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10842-102-01	237 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	05/10/2005
2	NDC: 10842-102-02	1814 mL in 1 JUG; Type 0: Not a Combination Product	05/10/2005
3	NDC: 10842-102-04	5 mL in 1 PACKET; Type 0: Not a Combination Product	05/10/2005
4	NDC: 10842-102-05	946 mL in 1 JUG; Type 0: Not a Combination Product	08/05/2015
5	NDC: 10842-102-08	89 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product	09/01/2015
6	NDC: 10842-102-09	3785 mL in 1 JUG; Type 0: Not a Combination Product	05/10/2005
7	NDC: 10842-102-03	118 mL in 1 TUBE; Type 0: Not a Combination Product	09/01/2015

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	05/10/2005

Labeler - DOCTOR HOY'S, LLC (791882322)

Registrant - DOCTOR HOY'S, LLC (791882322)