Multi-Strain Candida Relief NDC 57955-9998

NDC codes

FDA NDC Directory

Product NDC (as listed)57955-9998Labeler and product segments. Claims need a package NDC.

Product NDC at billing width57955-9998Add 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
57955-9998-2	57955999802	59 mL in 1 BOTTLE, SPRAY (57955-9998-2)Marketed from May 13, 2025

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): Multi-Strain Candida Relief
Generic name (nonproprietary): abies canadensis, agaricus muscarius, allium cepa, allium sativum, aloe, antimonium crudum, asafoetida, borax, candida albicans, candida parapsilosis, carpinus betulus, flos, ignatia amara, lachesis mutus, lycopodium clavatum, malus pumila, flos, olea europaea, flos, phosphoricum acidum, phytolacca decandra, pulsatilla, sabadilla, sticta pulmonaria, sulphur and thuja occidentalis
Active ingredients: Tsuga canadensis bark — 12 [hp_X]/59mLTsuga canadensis flower bud — 12 [hp_X]/59mLAmanita muscaria fruiting body — 12 [hp_X]/59mLOnion — 12 [hp_X]/59mLGarlic — 12 [hp_X]/59mLAloe — 12 [hp_X]/59mLAntimony trisulfide — 12 [hp_X]/59mLFerula assa-foetida resin — 12 [hp_X]/59mLSodium borate — 12 [hp_X]/59mLCandida albicans — 12 [hp_X]/59mLCandida parapsilosis — 12 [hp_X]/59mLCarpinus betulus flowering top — 12 [hp_X]/59mLStrychnos ignatii seed — 12 [hp_X]/59mLLachesis muta venom — 12 [hp_X]/59mLLycopodium clavatum spore — 12 [hp_X]/59mLMalus domestica flower — 12 [hp_X]/59mLOlea europaea flower — 12 [hp_X]/59mLPhosphoric acid — 12 [hp_X]/59mLPhytolacca americana root — 12 [hp_X]/59mLPulsatilla vulgaris whole — 12 [hp_X]/59mLSchoenocaulon officinale seed — 12 [hp_X]/59mLLobaria pulmonaria — 12 [hp_X]/59mLSulfur — 12 [hp_X]/59mLThuja occidentalis leafy twig — 12 [hp_X]/59mL
Dosage form: Liquid
Route: Oral
Labeler: King Bio Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: May 13, 2025
Listing expires: Dec 31, 2027
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Dietary Proteins (Chemical structure)Fungal Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Vegetable Proteins (Chemical structure)
Identifiers: Product ID 57955-9998_9a4c31c2-c1e8-4f33-8313-bfdb0ae68d69SPL ID 9a4c31c2-c1e8-4f33-8313-bfdb0ae68d69SPL set ID 02d4faa9-64e5-4d5a-9ba6-9d00a1d1e13fUNII R53V5F950S, Q3AW8FKK7X, DIF093I037, 492225Q21H, V1V998DC17, V5VD430YW9, F79059A38U, W9FZA51AS1, 91MBZ8H3QO, 4D7G21HDBC, 0KZ676D44N, QOI241B01F, 1NM3M2487K, VSW71SS07I, C88X29Y479, EF626V855K, 498M34P1VZ, E4GA8884NN, 11E6VI8VEG, I76KB35JEV, 6NAF1689IO, D1YM0P5Z2T, 70FD1KFU70, 1NT28V9397
Pharmacologic class: Non-Standardized Food Allergenic Extract; Non-Standardized Fungal 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

N457955999802 followed by a unit qualifier and the quantity

Package 57955-9998-02. 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 Mar 2, 2026.

Indications (excerpt from the label)

Uses † For temporary relief of: █ yeast infections █ thrush █ nausea █ nail fungus █ constipation █ cravings █ headache █ itchy scalp █ fatigue █ diarrhea █ flatulence █ forgetfulness █ sleeplessness

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)