FDA records indicate that there are no current recalls for this drug.
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Sterymine Pain Relief Recall
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Questions & Answers
Side Effects & Adverse Reactions
For external use only. direct patient not to ingest STERYMINE and to avoid contact with the eyes, mucous membranes, wounds, and damaged skin. If a rash develops, patient should discontinue use until rash clears. After the disappearance of rash, patient can try STERYMINE again on a test area and monitor the site for additional results. If no rash or redness results, then patient can resume use. However, if the rash persists or redevelops, use should be discontinued
Legal Issues
There is currently no legal information available for this drug.
FDA Safety Alerts
There are currently no FDA safety alerts available for this drug.
Manufacturer Warnings
There is currently no manufacturer warning information available for this drug.
FDA Labeling Changes
There are currently no FDA labeling changes available for this drug.
Uses
The drug is indicated for the relief of symptoms, including pain and inflammation associated with arthritis or trauma (such as sprains, strains, dislocations, repetitive/overuse injuries, traumatic, edema, post surgical edema, hematoma, general swelling of joints and soft tissues) to areas such as hand, wrist elbow, shoulder, neck, back, knees, ankles, feet and toes.
History
There is currently no drug history available for this drug.
Other Information
A homeopathic topical analgesic gel that contains the active ingredients indicated below in the corresponding concentrations.
Sources
Sterymine Pain Relief Manufacturers
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Pharmaceutica North America, Inc.
Sterymine Pain Relief | Pharmaceutica North America, Inc.
Apply a thin layer (1 drop covers an area of skin 2 inches by 2 inches) to the affected area 3-4 times daily and rub in gently. Applications of less than 3-4 times a day will not produce optimum results. Excess drops may be wiped from the area.
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