Doctor Hoys Natural Pain Relief
FDA Label NDC 10842-102

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Doctor Hoy's, Llc for the product Doctor Hoys Natural Pain Relief (NDC 10842-102). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding otc - active ingredient, otc - purpose, otc - keep out of reach of children, inactive ingredient, dosage & administration, indications & usage, warnings, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Otc - Active Ingredient

Active Ingredients      Purpose

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








Otc - Purpose

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

Otc - 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

Package Label.Principal Display Panel

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

 ID: MM1

Bottle Label (Label)

Bottle Label (Label)

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