FDA Label for Medicated Pain Relief
View Indications, Usage & Precautions
Medicated Pain Relief Product Label
The following document was submitted to the FDA by the labeler of this product Kareway Product, Inc.. 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
L-Menthol 5%
Purpose
Topical analgesic
Uses
Temporarily relieves minor arthritis pain, simple backache, bursitis tendonitis, muscle strains and sprains, bruises and cramps.
Warnings
For external use only
When Using This Product
- use only as directed
- do not bandage tightly or use a heating pad
- avoid contact with eyes and mucous membrane
- do not apply to wounds or damaged skin
Stop Use And Ask A Doctor If
- condition worsens
- symptoms persist for more than 7 days or clear up and occur again within a few days
- redness is present
- irritation develops
If Pregnant Or Breast-Feeding,
Ask a health professional before use.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Adults and children over 12 years:
- Carefully remove backing from patch
- Apply one patch to affected area
- Repeat as necessary, but no more than 4 times daily.
Inactive Ingredients
Purified Water, Acrylic Acid, Aluminum Hydroxide, Carboxymethylcellulose sodium, 2-Ethylhexyl Acrylate, Glycerin, Isopropyl Myristate, Methyl Acrylate, Nonoxymol-30, Sodium Polyacrylate, Polyacrylic Acid, Polysorbate 80, Sorbitan Sesquioleate, Starch, Talc, Tartaric acid, Titanium Dioxide
Package Label
Pain Relief Medicated Patch
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