VIVACITY- alfalfa, aralia quinquefolia, arnica montana, avena sativa, dna, galium aparine, hypericum perforatum, oleum animale, pituitarium posterium, rhus toxicodendron, rna, thuja occidentalis, alcohol, glycerin, water spray

Vivacity by

Drug Labeling and Warnings

Vivacity by is a Homeopathic medication manufactured, distributed, or labeled by Sunway Biotech LLC, Integra Health International, S.A. de C.V.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

INDICATIONS & USAGE

Indications: Temporarily relieves symptoms of general physical weakness and listlessness, including: fatigue; sore muscles & joints; dry skin; absence of sexual desire; occasional sleeplessness.

PURPOSE

NDC#: 2728100396

VIVACITY

Energy Medicine with DNA

Homeopathic Fast-Acting Oral Spray

1.0 Fl Oz (30 mL)

Alcohol 9% v/v

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

DOSAGE & ADMINISTRATION

Directions: Adults only: spray twice under the tongue, three times a day. This bottle contains about a 1 month supply.

WARNINGS

Warnings: Keep out of reach of children. If pregnant or breast feeding, ask a doctor before using product. Stop use and ask a doctor if symptoms persist more than 3 days, worsen, or if new symptoms occur.

OTHER SAFETY INFORMATION

Tamper Evident Seal: Do not use if seal around neck of bottle is broken or missing. The letters HPUS indicate that ingredients are officially included in the Homeopathic Pharmacopoeia of the United States.

Distributed by SUNWAY BIOTECH, LLC

Oak HIlls CA 92344 U.S.A. info@sunwaybiotech.com

ACTIVE INGREDIENT

Active Ingredients: Equal volumes of each ingredient: Alfalfa 2X HPUS, Aralia Quinquefolia 2X HPUS, Arnica Montana 3X HPUS, Avena Sativa 2X HPUS, DNA 6X HPUS, DNA 12X HPUS, Galium Aparine 3X HPUS, Hypericum Perforatum 200C HPUS, Oleum Animale 6X HPUS, Pituitarium Posterium 8X HPUS, Rhus Toxicodendron 200C HPUS, RNA 6X HPUS, Thuja Occidentalis 30C HPUS.

INACTIVE INGREDIENT

Inactive Ingredients: Alcohol 9% v/v, Glycerin 10% v/v, Purified Water.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

VIVACITY 
alfalfa, aralia quinquefolia, arnica montana, avena sativa, dna, galium aparine, hypericum perforatum, oleum animale, pituitarium posterium, rhus toxicodendron, rna, thuja occidentalis, alcohol, glycerin, water spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 27281-003
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALFALFA (UNII: DJO934BRBD) (ALFALFA - UNII:DJO934BRBD)	ALFALFA	1 [hp_C]  in 30 mL
ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW)	ARNICA MONTANA	1.5 [hp_C]  in 30 mL
AMERICAN GINSENG (UNII: 8W75VCV53Q) (AMERICAN GINSENG - UNII:8W75VCV53Q)	AMERICAN GINSENG	1 [hp_C]  in 30 mL
AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F) (AVENA SATIVA FLOWERING TOP - UNII:MA9CQJ3F7F)	AVENA SATIVA FLOWERING TOP	1 [hp_C]  in 30 mL
GALIUM APARINE (UNII: Z4B6561488) (GALIUM APARINE - UNII:Z4B6561488)	GALIUM APARINE	1.5 [hp_C]  in 30 mL
HERRING SPERM DNA (UNII: 51FI676N6F) (HERRING SPERM DNA - UNII:51FI676N6F)	HERRING SPERM DNA	3 [hp_C]  in 30 mL
HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (HYPERICUM PERFORATUM - UNII:XK4IUX8MNB)	HYPERICUM PERFORATUM	200 [hp_C]  in 30 mL
CERVUS ELAPHUS HORN OIL (UNII: 7A7G0PQI12) (CERVUS ELAPHUS HORN OIL - UNII:7A7G0PQI12)	CERVUS ELAPHUS HORN OIL	3 [hp_C]  in 30 mL
SUS SCROFA PITUITARY GLAND (UNII: E8S87O660T) (SUS SCROFA PITUITARY GLAND - UNII:E8S87O660T)	SUS SCROFA PITUITARY GLAND	4 [hp_C]  in 30 mL
TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (TOXICODENDRON PUBESCENS LEAF - UNII:6IO182RP7A)	TOXICODENDRON PUBESCENS LEAF	200 [hp_C]  in 30 mL
SACCHAROMYCES CEREVISIAE RNA (UNII: J17GBZ5VGX) (SACCHAROMYCES CEREVISIAE RNA - UNII:J17GBZ5VGX)	SACCHAROMYCES CEREVISIAE RNA	3 [hp_C]  in 30 mL
THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (THUJA OCCIDENTALIS LEAFY TWIG - UNII:1NT28V9397)	THUJA OCCIDENTALIS LEAFY TWIG	30 [hp_C]  in 30 mL

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 27281-003-01	30 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
2	NDC: 27281-003-02	60 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		11/13/2013

Labeler - Sunway Biotech LLC (019560802)

Establishment
Name	Address	ID/FEI	Business Operations
Integra Health International, S.A. de C.V.		589880301	manufacture(27281-003)