Arnica montana ARNICA MONTANA NEWTON LABORATORIES, INC. FDA Approved INDICATIONS & USAGE SECTION Trauma; Injuries; Bruises; Exhaustion; Headache; Sprains; Wounds
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Substance Arnica Montana
Route
ORAL
Package NDC

Drug Facts

Composition & Profile

Active Ingredients
OTC - ACTIVE INGREDIENT SECTION Arnica montana 30c.
Inactive Ingredients
INACTIVE INGREDIENT SECTION Inactive Ingredients: USP Purified Water; USP Gluten-free non-GMO organic cane alcohol 20%.
Treats Conditions
Indications Usage Section Trauma Injuries Bruises Exhaustion Headache Sprains Wounds

Identifiers & Packaging

Container Type UNKNOWN
All Product Codes
UNII
O80TY208ZW
Packaging

PACKAGE LABEL Package label

Package Descriptions
  • PACKAGE LABEL Package label

Overview

INDICATIONS & USAGE SECTION Trauma; Injuries; Bruises; Exhaustion; Headache; Sprains; Wounds

Indications & Usage

INDICATIONS & USAGE SECTION Trauma; Injuries; Bruises; Exhaustion; Headache; Sprains; Wounds

Dosage & Administration

DOSAGE & ADMINISTRATION SECTION Directions: Ages 12 and up, take 6 drops by mouth, (ages 0 to 11, give 3 drops) as needed or as directed by a health professional. Sensitive persons begin with 1 drop and gradually increase to full dose.

Warnings & Precautions
WARNINGS SECTION Warning: Keep out of reach of children. Do not use if tamper - evident seal is broken or missing. If symptoms worsen or persist for more than a few days, consult a doctor. If pregnant or breast-feeding, ask a doctor before use.
Purpose

OTC - PURPOSE SECTION Trauma; Injuries; Bruises; Exhaustion; Headache; Sprains; Wounds

Keep Out of Reach of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION Keep out of reach of children.

Questions

QUESTIONS SECTION newtonlabs.net – Questions? 800.448.7256 Newton Laboratories, Inc. FDA Est # 1051203 - Conyers, GA 30013


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