FDA Label for Banish My Pain
View Indications, Usage & Precautions
Banish My Pain Product Label
The following document was submitted to the FDA by the labeler of this product Laiden Montana Emu Products. 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
Camphor 4.6%
Purpose
Topical analgesic
Uses
for the temporary relief of minor aches and pains of muscles and joints associated with:
- simple backache
- arthritis
- strains
- bruises
- sprains
Warnings
For external use only.
Do Not Use
- on wounds or damaged skin
- with a heating pad
When Using This Product
- avoid contact with eyes and mucous membranes
- do not bandage tightly
Stop Use And Ask A Doctor If
- condition worsens
- symptoms persist for more than 7 days
- symptoms clear up and occur again within a few days
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 of age and older: Apply to affected area not more than 3 to 4 times daily.
- massage into area until thoroughly absorbed
- Children under 2 years of age: consult a doctor.
Other Information
- Best stored at room temperature or cooler.
Inactive Ingredients
Helianthus Annuus (Sunflower) Seed Oil, Emu Oil, Beeswax, Butyrospermum Parkii (Shea) Butter, Arnica Montana Flower, Calendula Officinalis (Calendula) Flower, Melissa Officinalis (Lemon Balm) Leaf, Chamomilla Recutita (Chamomile) Flower, Tocopherol, Melaleuca Leucadendron Cajaputi (Cajeput) Oil, Lavandula Angustifolia (Lavender) Oil, Eucalyptus Globulus (Eucalyptus) Leaf Oil, Chamomilla Recutita (Chamomile) Oil, Citrus Grandis (Grapefruit) Seed Extract.
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