Sterymine Pain Relief

Pharmaceutica North America, Inc.
Pharmaceutica North America, Inc.

Sterymine Pain Relief Gel

FULL PRESCRIBING INFORMATION: CONTENTS*

• Sterymine Pain Relief Gel
• STERYMINE PAIN RELIEF DESCRIPTION
• ACTIVE INGREDIENTS:
• INACTIVE INGREDIENTS:
• PHYSICAL INFORMATION
• CLINICAL PHARMACOLOGY
• STERYMINE PAIN RELIEF INDICATIONS AND USAGE
• STERYMINE PAIN RELIEF CONTRAINDICATIONS
• WARNINGS AND PRECAUTIONS
• OVERDOSAGE
• STERYMINE PAIN RELIEF ADVERSE REACTIONS
• Sterymine Pain Relief Gel 120g/4oz (45861-010-01)

FULL PRESCRIBING INFORMATION

Sterymine Pain Relief Gel

STERYMINE PAIN RELIEF DESCRIPTION

ACTIVE INGREDIENTS:

50 PARTS EACH: ECHINACEA ANGUSTIFOLIA 1X HPUS, ECHINACEA PUPUREA 1X HPUS, 30 PARTS: ACONITUM NAPELLUS 3X HPUS, 15 PARTS EACH: ARNICA MONTANA 3X HPUS, CALENDULA OFFICIANALIS 1X HPUS, HAMAMELIS VIRGINIANA 1X HPUS, 10 PARTS: BELLADONNA 3X HPUS, 5 PARTS EACH: BELLIS PERENNIS 1X HPUS, CHAMOMILLA 1X HPUS, 3 PARTS MILLEFOLIUM 1X HPUS, 1 PART EACH: HYPERICUM PERFORATUM 6X HPUS, SYMPHYTUM OFFICINALE 4X HPUS, .01 PART COLCHICINUM 3X HPUS

INACTIVE INGREDIENTS:

PURIFIED WATER, ISOPROPYL MYRISTATE, LECITHIN, UREA, DOCUSATE SODIUM, SODIUM HYDROXIDE

PHYSICAL INFORMATION

A clear amber colored, viscous gel with a slight floral smell.

CLINICAL PHARMACOLOGY

According to traditional homeopathic literature and Material Medica, the following ingredients provide the following attributes:

STERYMINE PAIN RELIEF INDICATIONS AND USAGE

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.

STERYMINE PAIN RELIEF CONTRAINDICATIONS

This drug should not be used by those sensitive to Arnica or any of the other listed ingredients.

WARNINGS AND PRECAUTIONS

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

Direct the patient to keep this product out of reach of children and seek medical help or contact a Poison Control Center immediately if swallowed.

In the homeopathic concentrations used to make STERYMINE, there are no known or expected interactions with other drugs or laboratory tests. In addition, the homeopathic concentrations used are below any levels with known or suspected toxicities

OVERDOSAGE

According to toxicology studies, a patient would have to orally ingest a minimum of 22 bottles of STERYMINE to experience any initial toxic effects.

STERYMINE PAIN RELIEF ADVERSE REACTIONS

Rarely, allergic skin reactions may occur. These effects are transient and will clear after a few days.

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.

Package size: 120gm (4 fl oz) bottle

NDC 45861-0010-01

STORE AT ROOM TEMPERATURE

Manufactured for

Pharmaceutica North America, Inc.

Glendale, CA 91204
877.328.2592
www.pnarx.com

Sterymine Pain Relief Gel 120g/4oz (45861-010-01)