Fungus Fighter NDC 55714-2556

NDC codes

FDA NDC Directory

Product NDC (as listed)55714-2556Labeler and product segments. Claims need a package NDC.

Product NDC at billing width55714-2556Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
55714-2556-1	55714255601	30 mL in 1 BOTTLE, GLASS (55714-2556-1)Marketed from Sep 2, 2019

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Fungus Fighter
Generic name (nonproprietary): 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.
Active ingredients: Silicon dioxide — 15 [hp_X]/mLSulfur — 15 [hp_X]/mLSulfuric acid — 15 [hp_X]/mLZinc — 15 [hp_X]/mLApis mellifera — 6 [hp_X]/mLThuja occidentalis leafy twig — 6 [hp_X]/mLCandida albicans — 15 [hp_X]/mLSanicula europaea leaf — 16 [hp_X]/mLTellurium — 16 [hp_X]/mLSaccharomyces cerevisiae — 16 [hp_X]/mLAntimony trisulfide — 15 [hp_X]/mLArsenic trioxide — 15 [hp_X]/mLBarium carbonate — 15 [hp_X]/mLBryonia alba root — 15 [hp_X]/mLOyster shell calcium carbonate, Crude — 15 [hp_X]/mLActivated charcoal — 15 [hp_X]/mLCopper — 15 [hp_X]/mLSolanum dulcamara top — 15 [hp_X]/mLGraphite — 15 [hp_X]/mLPotassium carbonate — 15 [hp_X]/mLLachesis muta venom — 15 [hp_X]/mLLycopodium clavatum spore — 15 [hp_X]/mLDaphne mezereum bark — 15 [hp_X]/mLNitric acid — 15 [hp_X]/mLPhosphorus — 15 [hp_X]/mLPhytolacca americana root — 15 [hp_X]/mLSepia officinalis juice — 15 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Newton Laboratories, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Sep 2, 2019
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Bee Venoms (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Copper (Chemical structure)Decreased Embryonic Implantation (Physiologic effect)Decreased Sperm Motility (Physiologic effect)Dietary Proteins (Chemical structure)Fungal Proteins (Chemical structure)Fungal Proteins (Chemical structure)Fungal Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Increased IgG Production (Physiologic effect)Increased IgG Production (Physiologic effect)Inhibit Ovum Fertilization (Physiologic effect)
Identifiers: Product ID 55714-2556_3cbdca22-0761-fa96-e063-6294a90ab116SPL ID 3cbdca22-0761-fa96-e063-6294a90ab116SPL set ID 93e05175-001b-c639-e053-2a95a90a289cUNII ETJ7Z6XBU4, 70FD1KFU70, O40UQP6WCF, J41CSQ7QDS, 7S82P3R43Z, 1NT28V9397, 4D7G21HDBC, JYZ6110L9I, NQA0O090ZJ, 978D8U419H, F79059A38U, S7V92P67HO, 6P669D8HQ8, T7J046YI2B, 2E32821G6I, 2P3VWU3H10, 789U1901C5, KPS1B1162N, 4QQN74LH4O, BQN1B9B9HA, VSW71SS07I, C88X29Y479, X2N6E405GV, 411VRN1TV4, 27YLU75U4W, 11E6VI8VEG, QDL83WN8C2
Pharmacologic class: Copper-containing Intrauterine Device; Non-Standardized Food Allergenic Extract; Non-Standardized Fungal Allergenic Extract; Standardized Insect Venom Allergenic Extract

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N455714255601 followed by a unit qualifier and the quantity

Package 55714-2556-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Aug 19, 2025.

Indications (excerpt from the label)

INDICATIONS & USAGE SECTION Formulated for symptoms such as itching, rashes, burning and eruptions associated with fungal infections of the nails, skin and scalp such as athlete's foot or ringworm.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)