SUPREN- arsenic trioxide, sulfuric acid, chamaelirium luteum root, goldenseal, wood creosote, lemna minor, magnesium fluoride, and silicon dioxide solution/ drops

SUPREN by

Drug Labeling and Warnings

SUPREN by is a Homeopathic medication manufactured, distributed, or labeled by PEKANA Naturheilmittel GmbH. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Ingredients:
Acidum arsenicosum	12X
Acidum sulfuricum	8X
Chamaelirium luteum	12X
Hydrastis canadensis	12X
Kreosotum	12X
Lemna minor	12X
Magnesium fluoratum	12X
Acidum silicicum (Silicea)	12X

Selected ingredients prepared by spagyric processes.

INACTIVE INGREDIENT

Contains 18% alcohol by volume.

Indications

For relief of occasional tiredness and weakness. Application of this homeopathic remedy for the designated usage is exclusively based on homeopathic experience. With severe forms of this disease, a clinically proven therapy is indicated.

Dosage

Unless otherwise prescribed, adults take 15-20 drops, 3 times per day. For pediatric dosages, consult your practitioner.

Warning

If symptoms persist, contact a licensed practitioner. If you have known sensitivity to any of the ingredients, please consult your licensed practitioner before use. If you are pregnant or nursing a baby, seek the advice of a health care professional before use.

Keep out of the reach of children.

Protect from light and heat.

Tamper Evident

Do not use this product if tamper evident strip is broken or removed from base of cap.

QUESTIONS

To report adverse events, contact BioResource at 321B Blodgett Street, Cotati, CA 94931

SPL UNCLASSIFIED SECTION

Distributed by:
BioResource Inc.
Cotati, CA 94931

Manufactured by:
PEKANA® GmbH
D-88353 Kisslegg

PRINCIPAL DISPLAY PANEL - 100 ml Bottle Box

SUPREN™
Oral Drops

Homeopathic Medicine

For relief of occasional
tiredness and weakness

3.34 FL OZ
(100 ml)

PEKANA®

INGREDIENTS AND APPEARANCE

SUPREN 
arsenic trioxide, sulfuric acid, chamaelirium luteum root, goldenseal, wood creosote, lemna minor, magnesium fluoride, and silicon dioxide solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59469-060
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Arsenic Trioxide (UNII: S7V92P67HO) (ARSENIC CATION (3+) - UNII:C96613F5AV)	Arsenic Trioxide	12 [hp_X]  in 100 mL
Sulfuric Acid (UNII: O40UQP6WCF) (Sulfuric Acid - UNII:O40UQP6WCF)	Sulfuric Acid	8 [hp_X]  in 100 mL
Chamaelirium luteum Root (UNII: DQV54Y5H3U) (Chamaelirium Luteum Root - UNII:DQV54Y5H3U)	Chamaelirium luteum Root	12 [hp_X]  in 100 mL
Goldenseal (UNII: ZW3Z11D0JV) (Goldenseal - UNII:ZW3Z11D0JV)	Goldenseal	12 [hp_X]  in 100 mL
Wood Creosote (UNII: 3JYG22FD73) (Wood Creosote - UNII:3JYG22FD73)	Wood Creosote	12 [hp_X]  in 100 mL
Lemna minor (UNII: 621HHM46SV) (Lemna minor - UNII:621HHM46SV)	Lemna minor	12 [hp_X]  in 100 mL
Magnesium fluoride (UNII: 5N014C7IWU) (Magnesium fluoride - UNII:5N014C7IWU)	Magnesium fluoride	12 [hp_X]  in 100 mL
Silicon Dioxide (UNII: ETJ7Z6XBU4) (Silicon Dioxide - UNII:ETJ7Z6XBU4)	Silicon Dioxide	12 [hp_X]  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Alcohol (UNII: 3K9958V90M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59469-060-10	1 in 1 BOX	04/12/2008
1		100 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
UNAPPROVED HOMEOPATHIC		04/12/2008

Labeler - PEKANA Naturheilmittel GmbH (320344542)

Establishment
Name	Address	ID/FEI	Business Operations
PEKANA Naturheilmittel GmbH		320344542	MANUFACTURE(59469-060)