YEAST FREEE- abies nigra, antimonium crudum, asafoetida, baptisia tinctoria, borax, candida albicans, lachesis mutus, phytolacca decandra, phosphoricum acidum, pulsatilla, sticta pulmonaria, sulphur, thuja occidentalis liquid

Yeast Freee by

Drug Labeling and Warnings

Yeast Freee by is a Homeopathic medication manufactured, distributed, or labeled by New Sun Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DOSAGE & ADMINISTRATION

Directions: Before initial dose depress pump 4-5 times or until primed and spray 1 dose directly in mouth 4 to 6 times daily until symptoms improve.

Adult Dose: 3 Pump Sprays

Child's Dose (2-12): 2 Pump Sprays

Infants - 2 yrs. 1 Pump Spray

WARNINGS

Warnings: If symptoms persist or worsen, seek advice of physician. If pregnant or breast-feeding, take only on advice of physician.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

OTHER SAFETY INFORMATION

Other information: Tamper resistant for your protection. Use only if safety seal is intact.

PURPOSE

Indications: For temporary relief of yeast or fungal overgrowths in both male and female, and the symptoms of: candida albicans, infections, fatigue, congestion, headaches, indigestion, poor bowel function, achy joints, poor memory, sensitive emotions, changing moods, mold sensitivity.

ACTIVE INGREDIENT

Active Ingredients: Abies nigra, Antimonium crudum, Asafoetida, Baptisia tinctoria, Borax, Candida albicans, Lachesis mutus, Phytolacca decandra, Phosphoricum acidum, Pulsatilla, Sticta pulmonaria, Sulphur, Thuja occidentalis. ​Equal volumes of each ingredient in 12X, 30X, 100X potencies.

INACTIVE INGREDIENT

Inactive Ingredient: Citric acid, potassium sorbate, purified water.

INDICATIONS & USAGE

Indications: For temporary relief of yeast or fungal overgrowths in both male and female, and the symptoms of:

• candida albicans
• infections
• fatigue
• congestion
• headaches
• indigestion
• poor bowel function
• achy joints
• poor memory
• sensitive emotions
• changing moods
• mold sensitivity

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

YEAST FREEE 
abies nigra, antimonium crudum, asafoetida, baptisia tinctoria, borax, candida albicans, lachesis mutus, phytolacca decandra, phosphoricum acidum, pulsatilla, sticta pulmonaria, sulphur, thuja occidentalis liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66579-0061
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PICEA MARIANA RESIN (UNII: 71AOV0W131) (PICEA MARIANA RESIN - UNII:71AOV0W131)	PICEA MARIANA RESIN	12 [hp_X]  in 59 mL
ANTIMONY TRISULFIDE (UNII: F79059A38U) (ANTIMONY TRISULFIDE - UNII:F79059A38U)	ANTIMONY TRISULFIDE	12 [hp_X]  in 59 mL
ASAFETIDA (UNII: W9FZA51AS1) (ASAFETIDA - UNII:W9FZA51AS1)	ASAFETIDA	12 [hp_X]  in 59 mL
BAPTISIA TINCTORIA ROOT (UNII: 5EF0HWI5WU) (BAPTISIA TINCTORIA ROOT - UNII:5EF0HWI5WU)	BAPTISIA TINCTORIA ROOT	12 [hp_X]  in 59 mL
SODIUM BORATE (UNII: 91MBZ8H3QO) (BORATE ION - UNII:44OAE30D22)	SODIUM BORATE	12 [hp_X]  in 59 mL
CANDIDA ALBICANS (UNII: 4D7G21HDBC) (CANDIDA ALBICANS - UNII:4D7G21HDBC)	CANDIDA ALBICANS	12 [hp_X]  in 59 mL
LACHESIS MUTA VENOM (UNII: VSW71SS07I) (LACHESIS MUTA VENOM - UNII:VSW71SS07I)	LACHESIS MUTA VENOM	12 [hp_X]  in 59 mL
PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (PHYTOLACCA AMERICANA ROOT - UNII:11E6VI8VEG)	PHYTOLACCA AMERICANA ROOT	12 [hp_X]  in 59 mL
PHOSPHORIC ACID (UNII: E4GA8884NN) (PHOSPHORIC ACID - UNII:E4GA8884NN)	PHOSPHORIC ACID	12 [hp_X]  in 59 mL
PULSATILLA VULGARIS (UNII: I76KB35JEV) (PULSATILLA VULGARIS - UNII:I76KB35JEV)	PULSATILLA VULGARIS	12 [hp_X]  in 59 mL
LOBARIA PULMONARIA (UNII: D1YM0P5Z2T) (LOBARIA PULMONARIA - UNII:D1YM0P5Z2T)	LOBARIA PULMONARIA	12 [hp_X]  in 59 mL
SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70)	SULFUR	12 [hp_X]  in 59 mL
THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (THUJA OCCIDENTALIS LEAFY TWIG - UNII:1NT28V9397)	THUJA OCCIDENTALIS LEAFY TWIG	12 [hp_X]  in 59 mL

Inactive Ingredients
Ingredient Name	Strength
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66579-0061-2	29 mL in 1 BOTTLE, SPRAY

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		08/19/2014

Labeler - New Sun Inc. (957251176)

Registrant - New Sun Inc. (957251176)