ROQUEFORTI- penicillium roqueforti liquid

Roqueforti by

Drug Labeling and Warnings

Roqueforti by is a Homeopathic medication manufactured, distributed, or labeled by USPharmaCo, DermaMed. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Homeopathic Medicine

Indications

For temporary relief from digestive discomfort

Dosage

5-10 drops, three times daily.

Active Ingredient

Penicillium roqueforti 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.

STORAGE AND HANDLING

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.

SPL UNCLASSIFIED SECTION

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

ROQUEFORTI DROPS 4X

Homeopathic Medicine 0.34 fl. oz. (10ml)

Indications: For temporary relief from digestive discomfort
Dosage: 5-10 drops, three times daily.
Active Ingredient: Penicillium roqueforti 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

INGREDIENTS AND APPEARANCE

ROQUEFORTI 
penicillium roqueforti liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49693-1801
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Penicillium roqueforti (UNII: 7ORP6R724L) (Penicillium roqueforti - UNII:7ORP6R724L)	Penicillium roqueforti	4 [hp_X]  in 10 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49693-1801-1	1 in 1 BOX
1		10 mL in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
UNAPPROVED HOMEOPATHIC		12/15/2009

Labeler - USPharmaCo (145322622)

Establishment
Name	Address	ID/FEI	Business Operations
DermaMed		256799461	MANUFACTURE