NDC 55714-2556 Fungus Fighter

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.

NDC Product Code 55714-2556

NDC Code: 55714-2556

Proprietary Name: Fungus Fighter What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary 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. What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

  • 55714 - Newton Laboratories, Inc.

NDC 55714-2556-1

Package Description: 30 mL in 1 BOTTLE, GLASS

NDC Product Information

Fungus Fighter with NDC 55714-2556 is a a human over the counter drug product labeled by Newton Laboratories, Inc.. The generic name of Fungus Fighter is 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.. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Newton Laboratories, Inc.

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Fungus Fighter Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • SILICON DIOXIDE 15 [hp_X]/mL
  • SULFUR 15 [hp_X]/mL
  • SULFURIC ACID 15 [hp_X]/mL
  • ZINC 15 [hp_X]/mL
  • APIS MELLIFERA 6 [hp_X]/mL
  • THUJA OCCIDENTALIS LEAFY TWIG 6 [hp_X]/mL
  • CANDIDA ALBICANS 15 [hp_X]/mL
  • SANICULA EUROPAEA LEAF 16 [hp_X]/mL
  • TELLURIUM 16 [hp_X]/mL
  • SACCHAROMYCES CEREVISIAE 16 [hp_X]/mL
  • ANTIMONY TRISULFIDE 15 [hp_X]/mL
  • ARSENIC TRIOXIDE 15 [hp_X]/mL
  • BARIUM CARBONATE 15 [hp_X]/mL
  • BRYONIA ALBA ROOT 15 [hp_X]/mL
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE 15 [hp_X]/mL
  • ACTIVATED CHARCOAL 15 [hp_X]/mL
  • COPPER 15 [hp_X]/mL
  • SOLANUM DULCAMARA TOP 15 [hp_X]/mL
  • GRAPHITE 15 [hp_X]/mL
  • POTASSIUM CARBONATE 15 [hp_X]/mL
  • LACHESIS MUTA VENOM 15 [hp_X]/mL
  • LYCOPODIUM CLAVATUM SPORE 15 [hp_X]/mL
  • DAPHNE MEZEREUM BARK 15 [hp_X]/mL
  • NITRIC ACID 15 [hp_X]/mL
  • PHOSPHORUS 15 [hp_X]/mL
  • PHYTOLACCA AMERICANA ROOT 15 [hp_X]/mL
  • SEPIA OFFICINALIS JUICE 15 [hp_X]/mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • ALCOHOL (UNII: 3K9958V90M)
  • WATER (UNII: 059QF0KO0R)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Newton Laboratories, Inc.
Labeler Code: 55714
Marketing Category: UNAPPROVED HOMEOPATHIC - What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 09-02-2019 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2020 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Fungus Fighter Product Label Images

Fungus Fighter Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

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) as needed 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. 15x, Arsenicum alb. 15x, Baryta carb. 15x, Bryonia 15x, Calc. carb.15x, Candida alb. 15x, Carbo veg. 15x, Cuprum met. 15x, Dulcamara 15x, Graphites 15x, Kali carb. 15x, Lachesis 15x, Lycopodium 15x, Mezereum 15x, Nitricum ac. 15x, Phos. 15x, Phytolacca 15x, Sepia 15x, Silicea 15x, Sulphur 15x, Sulphuricum ac. 15x, Zinc. met. 15x, Sanicula 16x, Tellurium 16x, Torula cerevisiae 16x.

Otc - Purpose Section

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

Inactive Ingredient Section

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

Questions Section

Newtonlabs.net – Questions? 800.448.7256Newton 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.

* Please review the disclaimer below.