Fungus Fighter

Manufacturer
Newton Laboratories, Inc.
Effective date
2019-01-31
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:09:28

Label at a glance#

ProductFungus Fighter
Active ingredientSILICON DIOXIDE, SULFUR, SULFURIC ACID, ZINC, APIS MELLIFERA, THUJA OCCIDENTALIS LEAFY TWIG, 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
Label structure9 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Formulated for symptoms associated with ringworm, athlete's foot and other fungal conditions of the nails, scalp and skin.

DOSAGE & ADMINISTRATION SECTION

Directions: Ages 12 and up, take 6 drops by mouth (ages 0 to 11, give 3 drops) one to four times daily or as directed by a health professional. Sensitive persons begin with 1 drop and gradually increase to full dose.

OTC - ACTIVE INGREDIENT SECTION

Equal parts of Apis mel. 6x, Phytolacca 6x, Thuja occ. 6x, Antimon. crud. 10x, Baryta carb. 10x, Bryonia 10x, Calc. carb.10x, Carbo veg. 10x, Cuprum met. 10x, Dulcamara 10x, Graphites 10x, Kali carb. 10x, Lachesis 10x, Lycopodium 10x, Mezereum 10x, Nitricum ac. 10x, Phos. 10x, Phytolacca 10x, Sepia 10x, Silicea 10x, Sulphur 10x, Sulphuricum ac. 10x, Zinc. met. 10x, Arsenicum alb. 15x, Candida alb. 15x, Sanicula 15x, Tellurium 15x, Torula cerevisiae 15x.

INACTIVE INGREDIENT SECTION

Inactive Ingredients: USP Purified Water; USP Gluten-free, non-GMO, organic cane alcohol 20%.

QUESTIONS SECTION

OTC - QUESTIONS SECTION

newtonlabs.net – Questions? 800.448.7256

Newton Laboratories, Inc. FDA Est # 1051203 - Conyers, GA 30013

WARNINGS SECTION

WARNINGS: Keep out of reach of children. Do not use if tamper-evident seal is broken or missing. If symptoms worsen or persist for more than a few days, consult a doctor. If pregnant or breast-feeding, ask a doctor before use.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a doctor before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

PACKAGE LABEL.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package LabelPackage Label

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55714-244655714-2446-1, 55714-2446-2, 55714-2446-0

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 29 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
93dd9395-b143-f369-e053-2a95a90a1e27924ed659-f916-6c2d-e053-2a95a90a32aa2019-10-01WarningsExact identifier
spl set id: 924ed659-f916-6c2d-e053-2a95a90a32aa

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.