AsperSAN by sanPharma GmbH AsperSAN

AsperSAN by

Drug Labeling and Warnings

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

Drug Details [pdf]

ASPERSAN- aspergillus niger var. niger 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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AsperSAN

Indications

For lymphatic stagnation

Dosage

5-10 drops, three times daily.

Ingredients

10ml Aspergillus niger 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

AsperSAN

Homeopathic
Medicine

For lymphatic
stagnation

0.34 FL OZ
(10ml)

san Pharma ®
biological health solutions

PRINCIAP DISPLAY PANEL - AsperSAN Drops

ASPERSAN 
aspergillus niger var. niger liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 64232-030
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6) ASPERGILLUS NIGER VAR. NIGER4 [hp_X]  in 10 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 64232-030-171 in 1 CARTON01/04/2017
110 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic01/04/201712/10/2019
Labeler - sanPharma GmbH (341409153)
Establishment
NameAddressID/FEIBusiness Operations
sanPharma GmbH341409153manufacture(64232-030) , label(64232-030)

Revised: 12/2019
 

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