RoquefoSAN by sanPharma GmbH RoquefoSAN

RoquefoSAN by

Drug Labeling and Warnings

RoquefoSAN by is a Homeopathic medication manufactured, distributed, or labeled by sanPharma GmbH. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ROQUEFOSAN- penicillium roqueforti liquid 
sanPharma GmbH

Disclaimer: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

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RoquefoSAN

Indications

For intestinal symptoms.

Dosage

5-10 drops, three times daily.

Ingredients

10ml Penicillium roqueforti 4X in a base of purified water, 0.09g sodium chloride, 0.01g 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 a baby, seek the advice of a health care professional before using this product.

Keep this and all medications out of the reach of children.

Protect from light and heat.

Tamper Evident

Do not use product if tamper evident strip is broken or removed from base of cap. To report adverse events, contact BioResource at 707/664-9023 or bioresource2@prodigy.net

Distributed By:
BioResource Inc.
Cotati CA 94931

PRINCIPAL DISPLAY PANEL - 10 ml Bottle Carton

RoquefoSAN

Homeopathic
Medicine

For intestinal
symptoms

0.34 FL OZ
(10ml)

san Pharma
biological health solutions

ROQUEFOSAN 
penicillium roqueforti liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 64232-035
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

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 64232-035-18	1 in 1 CARTON	02/01/2018
1		10 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		02/01/2018	12/10/2019

Labeler - sanPharma GmbH (341409153)

Establishment
Name	Address	ID/FEI	Business Operations
sanPharma GmbH		341409153	manufacture(64232-035) , label(64232-035)

Revised: 12/2019

Document Id: 995887da-f5f9-5306-e053-2a95a90a8cfc

34390-5

Set id: 500ef881-9a8e-4b80-9f8a-431fdb68e64e

Version: 4

Effective Time: 20191210