Mucor

USPharmaCo

MUCOR DROPS 4X

FULL PRESCRIBING INFORMATION: CONTENTS*

• Indications
• Dosage
• Active Ingredient
  • Inactive Ingredients
• Warning
• Tamper Evident
• PRINCIPAL DISPLAY PANEL - 10 ml Label

FULL PRESCRIBING INFORMATION

Homeopathic Medicine

Indications

For temporary relief of pain from bruises, sprains, and swelling of joints and muscles

Dosage

5-10. drops, three times daily.

Active Ingredient

Mucor racemosus 4X

Inactive Ingredients

Purified water, sodium chloride, potassium sorbate.

Warning

If symptoms persist more than a few days, contact a licensed practitioner. As with any drug, if you are pregnant or nursing, seek the advice of a health care professional before using this product.

Keep this and all medications out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Protect from light and heat.

Tamper Evident

Do not use product if the tamper evident strip is broken or removed from the base of the cap.

To report serious adverse events, call: 1-877-557-4276 or 1-623-582-3110

Manufactured for and distributed by:
USPharmaCo Distribution Ltd.
2205 W. Lone Cactus Drive #19,
Phoenix, AZ 85027
www.uspharmaco.com
info@uspharmaco.com

Made in Canada

PRINCIPAL DISPLAY PANEL - 10 ml Label

MUCOR DROPS 4X

Homeopathic Medicine 0.34 fl. oz. (10ml)

Indications: For temporary relief of pain from bruises, sprains, and swelling of joints and muscles
Dosage: 5-10 drops, three times daily.
Active Ingredient: Mucor racemosus 4X
Inactive Ingredients: Purified water, sodium chloride, potassium sorbate.
Warning: If symptoms persist more than a few days, contact a licensed practitioner. As with
any drug, if you are pregnant or nursing, seek the advice of a health care professional before
using this product. Keep this and all medications out of reach of children. In case of overdose,
get medical help or contact a Poison Control Center right away.Protect from light and heat.
Tamper Evident: Do not use product if the tamper evident strip is broken or removed from the
base of the cap.
To report serious adverse events, call: 1-877-557-4276 or 1-623-582-3110