SPRAYOLOGY WOMAN POWER- agnus castus, aralia quinquefolia, arnica montana, damiana, lactuca virosa, natrum muriaticum, onosmodium virginianum, oophorinum, phosphoricum acidum, pituitarum posterium, salix nigra, sepia, thuja occidentalis liquid

Sprayology Woman Power by

Drug Labeling and Warnings

Sprayology Woman Power by is a Homeopathic medication manufactured, distributed, or labeled by Eight and Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredients: Agnus castus 3X, Aralia quinquefolia 2X, Arnica montana 3X, Damiana 1X,2X, Lactuca virosa 3X, Natrum muriaticum 30C, Onosmodium virginianum 30C, Oophorinum 30C, Phosphoricum acidum 200C, Pituitarum posterium 12X, Salix nigra 3X, Sepia 30C, Thuja occidentalis 30C.

WARNINGS

Warnings: If symptoms persist or worsen, stop use and seek advice of physician. If pregnant or breast-feeding, ask a health care professional before use. Keep out of reach of children. Contains alcohol, in case of overdose, get medical help or contact a Poison Control Center right away.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

DOSAGE & ADMINISTRATION

Directions:

• For adult women only. 2 sprays under the tongue 3 times per day.

PURPOSE

Relieves temporarily the symptoms of low female energy, including:

• decreased dexual desire
• low physical energy
• irritability
• "the blues"

OTHER SAFETY INFORMATION

Other Information: Do not use if the transparent seal around spray bottle is broken or missing.

INACTIVE INGREDIENT

Inactive Ingredients: Glycerin 10% v/v, non-GMO organic alcohol 9% v/v, purified water.

INDICATIONS & USAGE

Relieves temporarily the symptoms of low female energy, including:

º decreased sexual desire

º low physical energy

º irritability

º "the blues"

° natural

° gluten free

° no artificial flavors or colors

° no known negative side effects

° no known negative drug interactions

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SPRAYOLOGY WOMAN POWER 
agnus castus, aralia quinquefolia, arnica montana, damiana, lactuca virosa, natrum muriaticum, onosmodium virginianum, oophorinum, phosphoricum acidum, pituitarum posterium, salix nigra, sepia, thuja occidentalis liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 61096-0034
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHASTE TREE (UNII: 433OSF3U8A) (CHASTE TREE - UNII:433OSF3U8A)	CHASTE TREE	3 [hp_X]  in 41 mL
AMERICAN GINSENG (UNII: 8W75VCV53Q) (AMERICAN GINSENG - UNII:8W75VCV53Q)	AMERICAN GINSENG	2 [hp_X]  in 41 mL
ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW)	ARNICA MONTANA	3 [hp_X]  in 41 mL
TURNERA DIFFUSA LEAFY TWIG (UNII: RQ2CFA7WWJ) (TURNERA DIFFUSA LEAFY TWIG - UNII:RQ2CFA7WWJ)	TURNERA DIFFUSA LEAFY TWIG	2 [hp_X]  in 41 mL
LACTUCA VIROSA (UNII: 6D74QW4H67) (LACTUCA VIROSA - UNII:6D74QW4H67)	LACTUCA VIROSA	3 [hp_X]  in 41 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698)	SODIUM CHLORIDE	30 [hp_C]  in 41 mL
ONOSMODIUM VIRGINIANUM WHOLE (UNII: 604NK4250S) (ONOSMODIUM VIRGINIANUM WHOLE - UNII:604NK4250S)	ONOSMODIUM VIRGINIANUM WHOLE	30 [hp_C]  in 41 mL
SUS SCROFA OVARY (UNII: S7YTV04R8O) (SUS SCROFA OVARY - UNII:S7YTV04R8O)	SUS SCROFA OVARY	30 [hp_C]  in 41 mL
PHOSPHORIC ACID (UNII: E4GA8884NN) (PHOSPHORIC ACID - UNII:E4GA8884NN)	PHOSPHORIC ACID	200 [hp_C]  in 41 mL
SUS SCROFA PITUITARY GLAND (UNII: E8S87O660T) (SUS SCROFA PITUITARY GLAND - UNII:E8S87O660T)	SUS SCROFA PITUITARY GLAND	12 [hp_X]  in 41 mL
SALIX NIGRA BARK (UNII: QU52J3A5B3) (SALIX NIGRA BARK - UNII:QU52J3A5B3)	SALIX NIGRA BARK	3 [hp_X]  in 41 mL
SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2) (SEPIA OFFICINALIS JUICE - UNII:QDL83WN8C2)	SEPIA OFFICINALIS JUICE	30 [hp_C]  in 41 mL
THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (THUJA OCCIDENTALIS LEAFY TWIG - UNII:1NT28V9397)	THUJA OCCIDENTALIS LEAFY TWIG	30 [hp_C]  in 41 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 61096-0034-1	1 in 1 CARTON
1		41 mL in 1 BOTTLE, SPRAY

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		02/05/2014

Labeler - Eight and Company (927364120)

Registrant - Eight and Company (927364120)