FDA Label for Arnica Pain Relief
View Indications, Usage & Precautions
Arnica Pain Relief Product Label
The following document was submitted to the FDA by the labeler of this product Magni Group. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Active Ingredient
Mountain arnica (Arnica montana) 3X HPUS
The letters 'HPUS' indicate thant the component in this product is officially monographed in the Homoeopathic Pharmacopoeia of the United States.
Purpose
Pain reliever
Use
temporarily relieves minor aches and pains associated with sore muscles, joint discomfort, strains, sprains, arthritis, and bruises.
Warnings
For external use only.
Avoid contact with eyes.
Do Not Use
- on open wounds
- cuts
- damaged skin
- infected skin.
Stop Use And Ask A Doctor If
symptoms persist for more than 7 days or worsens.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
- Adults and children 2 years and above:
- Apply a thin layer to affected area and surrounding areas as soon as possible after injury.
- Lightly rub in and reapply after 30 seconds.
- Repeat 4 times a day for 3 to 5 days.
- When pain has subsided, apply once each morning and evening for continued temporary relief.
Other Information:
Store tightly closed in a cool, dry place.
Inactive Ingredients
Aloe vera leaf juice, benzoic acid, carbomer 940, emu oil, eucalyptus oil, glycerin, PEG-40 hydrogenated castor oil, phenoxyethanol, sodium hydroxide, sorbic acid
Package Labeling:
* Please review the disclaimer below.
