Total Body Detox NDC 57955-9981

NDC codes

FDA NDC Directory

Product NDC (as listed)57955-9981Labeler and product segments. Claims need a package NDC.

Product NDC at billing width57955-9981Add 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
57955-9981-2	57955998102	59 mL in 1 BOTTLE, SPRAY (57955-9981-2)Marketed from Mar 15, 2026

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): Total Body Detox
Generic name (nonproprietary): alumina, bryonia, calcarea iodata, cantharis, carduus benedictus, carduus mar, chelidonium maj, cinchona officinalis, cynara scolymus, dioscorea villosa, hepar sulphuris calcareum, iris versicolor, juniperus communis, kali iodatum, mercurius corrosivus, mercurius vivus, natrum carbonicum, nux vomica, plumbum metallicum, ptelea trifoliata, ricinus communis, robinia pseudoacacia, serum anguillae, solidago virgaurea, sulphur, sulphuricum acidum and taraxacum officinale.
Active ingredients: Aluminum oxide — 10 [hp_X]/59mLBryonia alba root — 10 [hp_X]/59mLCalcium iodide — 10 [hp_X]/59mLLytta vesicatoria — 10 [hp_X]/59mLCentaurea benedicta — 10 [hp_X]/59mLMilk thistle — 10 [hp_X]/59mLChelidonium majus whole — 10 [hp_X]/59mLCinchona officinalis bark — 10 [hp_X]/59mLCynara scolymus leaf — 10 [hp_X]/59mLDioscorea villosa tuber — 10 [hp_X]/59mLCalcium sulfide — 10 [hp_X]/59mLIris versicolor root — 10 [hp_X]/59mLJuniper berry — 10 [hp_X]/59mLPotassium iodide — 10 [hp_X]/59mLMercuric chloride — 10 [hp_X]/59mLMercury — 10 [hp_X]/59mLSodium carbonate — 10 [hp_X]/59mLStrychnos nux-vomica seed — 10 [hp_X]/59mLLead — 10 [hp_X]/59mLPtelea trifoliata bark — 10 [hp_X]/59mLRicinus communis seed — 10 [hp_X]/59mLRobinia pseudoacacia bark — 10 [hp_X]/59mLAnguilla rostrata blood serum — 10 [hp_X]/59mLSolidago virgaurea flowering top — 10 [hp_X]/59mLSulfur — 10 [hp_X]/59mLSulfuric acid — 10 [hp_X]/59mLTaraxacum officinale — 10 [hp_X]/59mL
Dosage form: Liquid
Route: Oral
Labeler: King Bio Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Mar 15, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)Calcium (Chemical structure)Divalent (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Food Additives (Chemical structure)Increased Coagulation Factor Activity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Phosphate Chelating Activity (Mechanism)Plant Proteins (Chemical structure)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 57955-9981_d3ffa4b2-eefb-4910-b8f9-b7a66184042fSPL ID d3ffa4b2-eefb-4910-b8f9-b7a66184042fSPL set ID c803733e-b5e2-46f2-bdfe-b239f38d9312UNII LMI26O6933, T7J046YI2B, 8EKI9QEE2H, 3Q034RO3BT, 6L5ZL09795, U946SH95EE, 7E889U5RNN, S003A158SB, B71UA545DE, IWY3IWX2G8, 1MBW07J51Q, X43D4L3DQC, O84B5194RL, 1C4QK22F9J, 53GH7MZT1R, FXS1BY2PGL, 45P3261C7T, 269XH13919, 2P299V784P, 5KQR6FTT0D, 7EK4SFN1TX, 7TPC058OWY, L7B16ESD1U, 5405K23S50, 70FD1KFU70, O40UQP6WCF, 39981FM375
Pharmacologic class: Blood Coagulation Factor; Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract; Phosphate Binder

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

N457955998102 followed by a unit qualifier and the quantity

Package 57955-9981-02. 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 4, 2026.

Indications (excerpt from the label)

Uses † For temporary relief of: diarrhea indigestion mental fogginess insomnia urinary tract imbalances † Claims based on traditional Homeopathic practice, not accepted medical evidence, not FDA evaluated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)