Search by Drug Name or NDC

NDC 50181-0059-01 BioTox DIP 6; 6; 6; 6; 6; 6; 6; 6; 6; 6 [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL Details

BioTox DIP 6; 6; 6; 6; 6; 6; 6; 6; 6; 6 [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL

BioTox DIP is a ORAL LIQUID in the HUMAN OTC DRUG category. It is labeled and distributed by The Wellness Center For Research and Education. The primary component is ACONITUM NAPELLUS; ARSENIC TRIOXIDE; DIBASIC POTASSIUM PHOSPHATE; LACHESIS MUTA VENOM; LYCOPODIUM CLAVATUM SPORE; MERCURIC CYANIDE; PHYTOLACCA AMERICANA ROOT; POTASSIUM CHLORIDE; POTASSIUM DICHROMATE; TOXICODENDRON PUBESCENS LEAF.

Product Information

NDC	50181-0059
Product ID	50181-0059_41964e1b-bfe5-41a7-a0c7-55607148d506
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	BioTox DIP
Proprietary Name Suffix	n/a
Non-Proprietary Name	Aconitum Napellus, Arsenicum Album, Kali Bichromicum, Kali Muriaticum, Kali Phosphoricum, Lachesis Mutus, Lycopodium Clavatum, Mercurius Cyanatus, Phytolacca Decandra, Rhus Tox
Product Type	HUMAN OTC DRUG
Dosage Form	LIQUID
Route	ORAL
Active Ingredient Strength	6; 6; 6; 6; 6; 6; 6; 6; 6; 6
Active Ingredient Units	[hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL
Substance Name	ACONITUM NAPELLUS; ARSENIC TRIOXIDE; DIBASIC POTASSIUM PHOSPHATE; LACHESIS MUTA VENOM; LYCOPODIUM CLAVATUM SPORE; MERCURIC CYANIDE; PHYTOLACCA AMERICANA ROOT; POTASSIUM CHLORIDE; POTASSIUM DICHROMATE; TOXICODENDRON PUBESCENS LEAF
Labeler Name	The Wellness Center For Research and Education
Pharmaceutical Class	Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC]
DEA Schedule	n/a
Marketing Category	UNAPPROVED HOMEOPATHIC
Application Number	n/a
Listing Certified Through	2024-12-31

Package

Package Images

NDC 50181-0059-01 (50181005901)

Pricing Information	N/A
NDC Package Code	50181-0059-1
Billing NDC	50181005901
Package	30 mL in 1 BOTTLE, DROPPER (50181-0059-1)
Marketing Start Date	2018-03-16
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL d5db8bd2-9ea2-49bf-9b6e-d26d9f841d81 Details

ACTIVE INGREDIENTS:

Aconitum Napellus 6C, 12C, 30C, 1LM, Arsenicum Album 6C, 12C, 30C, 1LM, Kali Bichromicum 6C, 12C, 30C, 1LM, Kali Muriaticum 6C, 12C, 30C, 1LM, Kali Phosphoricum 6C, 12C, 30C, 1LM, Lachesis Mutus 6C, 12C, 30C, 1LM, Lycopodium Clavatum 6C, 12C, 30C, 1LM, Mercurius Cyanatus 6C, 12C, 30C, 1LM, Phytolacca Decandra 6C, 12C, 30C, 1LM, Rhus Tox 6C, 12C, 30C, 1LM.

INDICATIONS:

Whole body chills, fatigue, fever, or malaise. Noisy breathing or shortness of breath. Rashes or ulcers. Hoarseness or impaired voice. Difficulty swallowing. Coughing, muscle weakness, runny nose, swelling, or swollen lymph nodes.

WARNINGS:

If you are pregnant or breastfeeding, ask a health professional before using this product.

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Do not use if tamper evident seal is broken or missing.

KEEP OUT OF REACH OF CHILDREN:

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

DIRECTIONS:

5 drops orally 2 times per day, 1 to 5 days per week, depending on symptoms and provider recommendations. Consult a physician for use in children under 12 years of age.

INDICATIONS:

INACTIVE INGREDIENTS:

Demineralized Water, 25% Ethanol

QUESTIONS:

MFD FOR: The Wellness Center for

Research and Education, Inc.,

1237 S. Victoria, Suite 169

Oxnard, CA 93035 1-866-962-6484

PACKAGE LABEL DISPLAY:

Dr. Theresa Dale's

NDC 50181-0059-1

Homeopathic

BioTox

DIP

1 fl oz (30 ml)

INGREDIENTS AND APPEARANCE

BIOTOX DIP

aconitum napellus, arsenicum album, kali bichromicum, kali muriaticum, kali phosphoricum, lachesis mutus, lycopodium clavatum, mercurius cyanatus, phytolacca decandra, rhus tox liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:50181-0059
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ACONITUM NAPELLUS (UNII: U0NQ8555JD) (ACONITUM NAPELLUS - UNII:U0NQ8555JD)	ACONITUM NAPELLUS	6 [hp_C] in 1 mL
ARSENIC TRIOXIDE (UNII: S7V92P67HO) (ARSENIC CATION (3+) - UNII:C96613F5AV)	ARSENIC TRIOXIDE	6 [hp_C] in 1 mL
POTASSIUM DICHROMATE (UNII: T4423S18FM) (DICHROMATE ION - UNII:9LKY4BFN2V)	POTASSIUM DICHROMATE	6 [hp_C] in 1 mL
POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152)	POTASSIUM CATION	6 [hp_C] in 1 mL
DIBASIC POTASSIUM PHOSPHATE (UNII: CI71S98N1Z) (PHOSPHATE ION - UNII:NK08V8K8HR)	DIBASIC POTASSIUM PHOSPHATE	6 [hp_C] in 1 mL
LACHESIS MUTA VENOM (UNII: VSW71SS07I) (LACHESIS MUTA VENOM - UNII:VSW71SS07I)	LACHESIS MUTA VENOM	6 [hp_C] in 1 mL
LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (LYCOPODIUM CLAVATUM SPORE - UNII:C88X29Y479)	LYCOPODIUM CLAVATUM SPORE	6 [hp_C] in 1 mL
MERCURIC CYANIDE (UNII: RWG7BD1032) (MERCURIC CYANIDE - UNII:RWG7BD1032)	MERCURIC CYANIDE	6 [hp_C] in 1 mL
PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (PHYTOLACCA AMERICANA ROOT - UNII:11E6VI8VEG)	PHYTOLACCA AMERICANA ROOT	6 [hp_C] in 1 mL
TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (TOXICODENDRON PUBESCENS LEAF - UNII:6IO182RP7A)	TOXICODENDRON PUBESCENS LEAF	6 [hp_C] in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:50181-0059-1	30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	03/16/2018

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		03/16/2018

Labeler - The Wellness Center For Research and Education (832363993)

Registrant - Apotheca Company (844330915)

Name	Address	ID/FEI	Business Operations
Establishment
Apotheca Company		844330915	manufacture(50181-0059) , api manufacture(50181-0059) , label(50181-0059) , pack(50181-0059)

Revised: 3/2018

Document Id: 41964e1b-bfe5-41a7-a0c7-55607148d506

Set id: d5db8bd2-9ea2-49bf-9b6e-d26d9f841d81

Version: 1

Effective Time: 20180316

Search by Drug Name or NDC

NDC 50181-0059-01 BioTox DIP 6; 6; 6; 6; 6; 6; 6; 6; 6; 6 [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL Details

BioTox DIP 6; 6; 6; 6; 6; 6; 6; 6; 6; 6 [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL

Product Information

Package

Package Images

NDC 50181-0059-01 (50181005901)

Contents

Standard Product Labeling (SPL)/Prescribing Information SPL d5db8bd2-9ea2-49bf-9b6e-d26d9f841d81 Details

ACTIVE INGREDIENTS:

INDICATIONS:

WARNINGS:

KEEP OUT OF REACH OF CHILDREN:

DIRECTIONS:

INDICATIONS:

INACTIVE INGREDIENTS:

QUESTIONS:

PACKAGE LABEL DISPLAY:

INGREDIENTS AND APPEARANCE

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