SubtiSAN by sanPharma GmbH SubtiSAN

SubtiSAN by

Drug Labeling and Warnings

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

Drug Details [pdf]

SUBTISAN- bacillus subtilis 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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SubtiSAN

Indications

For infections, colds and immune support.

Dosage

5-10 drops, two times weekly.

Ingredients

10ml Bacillus subtilis 6X 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

SubtiSAN

Homeopathic
Medicine

For infections,
colds and immune
support

0.34 FL OZ
(10ml)

san Pharma
biological health solutions

SUBTISAN 
bacillus subtilis liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 64232-018
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BACILLUS SUBTILIS (UNII: 8CF93KW41W) (BACILLUS SUBTILIS - UNII:8CF93KW41W)	BACILLUS SUBTILIS	6 [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: 64232-018-03	1 in 1 CARTON	01/09/2018
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		01/09/2018	12/10/2019

Labeler - sanPharma GmbH (341409153)

Establishment
Name	Address	ID/FEI	Business Operations
sanPharma GmbH		341409153	manufacture(64232-018) , label(64232-018)

Revised: 12/2019

Document Id: 995792f6-d680-db60-e053-2995a90ad154

34390-5

Set id: 267afcc4-cfe1-4b8b-b18f-fa035e396db6

Version: 4

Effective Time: 20191210

 

sanPharma GmbH