Fungus Fighter

Product NDC

55714-2226

11-digit product format

557142226

Labeler code

55714

Product ID

55714-2226_0ba48a10-49f5-bf35-ccca-335bf1b5c4eb

Type

HUMAN OTC DRUG

Nonproprietary name

Candida albicans, Sanicula, Tellurium metallicum, Torula cerevisiae, Antimon. crud., Arsenicum alb., Baryta carb., Bryonia, Calc. carb., Carbo veg., Cuprum met., Dulcamara, Graphites, Kali carb., Lachesis, Lycopodium, Mezereum, Nitricum ac., Phosphorus, Phytolacca, Sepia, Silicea, Sulphur, Sulphuricum ac., Zinc. met., Apis mel., Thuja occ.

Dosage form

LIQUID

Route

ORAL

Labeler

Newton Laboratories, Inc.

Marketing category

UNAPPROVED HOMEOPATHIC

Marketing start

2011-03-01

Marketing end

0000-00-00

Substance

CANDIDA ALBICANS; SANICULA EUROPAEA LEAF; TELLURIUM; SACCHAROMYCES CEREVISIAE; ANTIMONY TRISULFIDE; ARSENIC TRIOXIDE; BARIUM CARBONATE; BRYONIA ALBA ROOT; OYSTER SHELL CALCIUM CARBONATE, CRUDE; ACTIVATED CHARCOAL; COPPER; SOLANUM DULCAMARA TOP; GRAPHITE; POTASSIUM CARBONATE; LACHESIS MUTA VENOM; LYCOPODIUM CLAVATUM SPORE; DAPHNE MEZEREUM BARK; NITRIC ACID; PHOSPHORUS; PHYTOLACCA AMERICANA ROOT; SEPIA OFFICINALIS JUICE; SILICON DIOXIDE; SULFUR; SULFURIC ACID; ZINC; APIS MELLIFERA; THUJA OCCIDENTALIS LEAFY TWIG

Active strength

15 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record