THYMUS (thymus- suis liquid

THYMUS by

Drug Labeling and Warnings

THYMUS by is a Homeopathic medication manufactured, distributed, or labeled by BioActive Nutrional, Inc., Apotheca Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS:

Thymus (Suis) 8X.

INDICATIONS:

Regulation and stimulation of the Thymus Gland. For temporary relief of symptoms due to lowered immune response, viral infections, or influenza.

WARNINGS:

​If pregnant or breast-feeding,​ ask a health care professional before use.

​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.

Store in a cool, dry place.

DIRECTIONS:

Three sprays per day. Hold in mouth for three minutes.

INACTIVE INGREDIENTS:

Citric Acid, Demineralized Water, Glycerin, Sodium Benzoate.

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.

INDICATIONS:

Regulation and stimulation of the Thymus Gland. For temporary relief of symptoms due to lowered immune response, viral infections, or influenza.

QUESTIONS:

Distributed by:

BIOACTIVE NUTRITIONAL

Melbourne, FL 32935

For Nutritional Information write:

BioActive Nutritional, Inc.

1803 N. Wickham Rd.

Melbourne, FL 32935

PACKAGE LABEL DISPLAY:

BIOActive Nutritional

THYMUS

HOMEOPATHIC

1 FL OZ (30 ml)

INGREDIENTS AND APPEARANCE

THYMUS 
thymus (suis) liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 43857-0194
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SUS SCROFA THYMUS (UNII: 7B69B0BD62) (SUS SCROFA THYMUS - UNII:7B69B0BD62)	SUS SCROFA THYMUS	8 [hp_X]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM BENZOATE (UNII: OJ245FE5EU)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 43857-0194-1	30 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	12/06/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		08/09/2013

Labeler - BioActive Nutrional, Inc. (624980496)

Registrant - Apotheca Company (844330915)

Establishment
Name	Address	ID/FEI	Business Operations
Apotheca Company		844330915	manufacture(43857-0194) , api manufacture(43857-0194) , label(43857-0194) , pack(43857-0194)