FUNGUS- graphite - sepia officinalis juice - sulfur - thuja occidentalis leafy twig pellet

Fungus by

Drug Labeling and Warnings

Fungus by is a Homeopathic medication manufactured, distributed, or labeled by Washington Homeopathic Products. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS

GRAPHITES    6C

SEPIA    6C

SULPHUR       6C

THUJA   6C

USES

To relieve the symptoms of burning and itching eruptions of the skin, as in ringworm or athlete’s foot.

KEEP OUT OF REACH OF CHILDREN

Keep this and all medicines out of reach of children.

INDICATIONS

Indications:

GRAPHITES    Cracks in skin

SEPIA   Indifference

SULPHUR       Skin problems

THUJA   Warts

STOP USE AND ASK DOCTOR

If symptoms persist/worsen or if pregnant/nursing, stop use and consult your practitioner.

DIRECTIONS

Adults 2 pellets every 3 hours for 2 days. Then 2 pellets morning and night for 2 weeks.

Children: 1 pellet. Repeat as necessary.

INACTIVE INGREDIENTS

Sucrose/Lactose

PRINCIPAL DISPLAY PANEL

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INGREDIENTS AND APPEARANCE

FUNGUS 
graphite - sepia officinalis juice - sulfur - thuja occidentalis leafy twig pellet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 68428-009
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GRAPHITE (UNII: 4QQN74LH4O) (GRAPHITE - UNII:4QQN74LH4O)	GRAPHITE	6 [hp_C]  in 28 g
SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2) (SEPIA OFFICINALIS JUICE - UNII:QDL83WN8C2)	SEPIA OFFICINALIS JUICE	6 [hp_C]  in 28 g
SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70)	SULFUR	6 [hp_C]  in 28 g
THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (THUJA OCCIDENTALIS LEAFY TWIG - UNII:1NT28V9397)	THUJA OCCIDENTALIS LEAFY TWIG	6 [hp_C]  in 28 g

Inactive Ingredients
Ingredient Name	Strength
SUCROSE (UNII: C151H8M554)
LACTOSE (UNII: J2B2A4N98G)

Product Characteristics
Color	white (white)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 68428-009-14	28 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/07/2010

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		07/07/2010

Labeler - Washington Homeopathic Products (084929389)

Establishment
Name	Address	ID/FEI	Business Operations
Washington Homeopathic Products		084929389	manufacture(68428-009)