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 suppository 
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.

Ingredients

182mg Aspergillus niger 3X with sodium chloride in a base of mono-, di-, triglycerides (hard fat).

Dosage

Insert one suppository rectally each night before bed.

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

Use this product only if inner blister pack is intact. 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 Suppository Blister Pack Box

AsperSAN

Homeopathic Medicine

For lymphatic stagnation

10 Suppositories

sanPharma ®
biological health solutions

ASPERSAN 
aspergillus niger var. niger suppository

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 64232-029
Route of Administration	RECTAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ASPERGILLUS NIGER VAR. NIGER (UNII: 9IOA40ANG6) (ASPERGILLUS NIGER VAR. NIGER - UNII:9IOA40ANG6)	ASPERGILLUS NIGER VAR. NIGER	3 [hp_X]

Inactive Ingredients
Ingredient Name	Strength
FAT, HARD (UNII: 8334LX7S21)
WATER (UNII: 059QF0KO0R)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 64232-029-17	2 in 1 BOX	12/01/2017
1		5 in 1 BLISTER PACK; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		12/01/2017	12/10/2019

Labeler - sanPharma GmbH (341409153)

Establishment
Name	Address	ID/FEI	Business Operations
sanPharma GmbH		341409153	manufacture(64232-029) , label(64232-029)

Revised: 12/2019

Document Id: 99587e7a-1e22-4d15-e053-2a95a90a67d7

34390-5

Set id: 40e8eb63-9d23-47e4-a9a4-fd939dbf6bcf

Version: 3

Effective Time: 20191210

 

sanPharma GmbH