CandidaSAN by sanPharma GmbH CandidaSAN

CandidaSAN by

Drug Labeling and Warnings

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

Drug Details [pdf]

CANDIDASAN- candida parapsilosis 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.

----------

CandidaSAN

Indications

For relief of yeast infections.

Dosage

5-10 drops, three times daily.

Ingredients

10ml Candida parapsilosis 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

CandidaSAN

Homeopathic
Medicine

For yeast infections

0.34 FL OZ
(10ml)

san Pharma
biological health solutions

PRINCIPAL DISPLAY PANEL - 10 ml Bottle Carton
CANDIDASAN 
candida parapsilosis liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 64232-026
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CANDIDA PARAPSILOSIS (UNII: 0KZ676D44N) (CANDIDA PARAPSILOSIS - UNII:0KZ676D44N) CANDIDA PARAPSILOSIS4 [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: 64232-026-031 in 1 CARTON07/09/2018
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 homeopathic01/09/201812/10/2019
Labeler - sanPharma GmbH (341409153)
Establishment
NameAddressID/FEIBusiness Operations
sanPharma GmbH341409153manufacture(64232-026) , label(64232-026)

Revised: 12/2019
 

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.