NDC codes

FDA NDC Directory
Product NDC (as listed)43857-0613Labeler and product segments. Claims need a package NDC.
Product NDC at billing width43857-0613Add 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 NDC11-digit (billing)PackageCopy
43857-0613-14385706130130 mL in 1 PACKAGE (43857-0613-1)Marketed from Sep 2, 2021

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)
Bio Chem Detox
Generic name (nonproprietary)
berberis vulgaris, glycyrrhiza glabra, lappa major, rhamnus purshiana, stillingia sylvatica, trifolium pratense, triticum aestivum, xanthoxylum fraxineum, phytolacca decandra, glandula suprarenalis suis, hepar suis, lymph node (suis), thyroidinum (suis), lycopodium clavatum, nux vomica, phosphoricum acidum, aconitum napellus, arsenicum album, belladonna, carbo vegetabilis, cinchona officinalis, conium maculatum, mercurius corrosivus, phosphorus, sulphur, tabacum, nitricum acidum, agaricus muscarius,
Active ingredients
Berberis vulgaris root bark — 3 [hp_X]/mLGlycyrrhiza glabra — 3 [hp_X]/mLArctium lappa root — 3 [hp_X]/mLFrangula purshiana bark — 3 [hp_X]/mLStillingia sylvatica root — 3 [hp_X]/mLTrifolium pratense flower — 3 [hp_X]/mLTriticum aestivum whole — 3 [hp_X]/mLZanthoxylum americanum bark — 3 [hp_X]/mLPhytolacca americana root — 4 [hp_X]/mLSus scrofa adrenal gland — 6 [hp_X]/mLPork liver — 6 [hp_X]/mLSus scrofa lymph — 6 [hp_X]/mLThyroid — 6 [hp_X]/mLLycopodium clavatum spore — 12 [hp_X]/mLStrychnos nux-vomica seed — 12 [hp_X]/mLPhosphoric acid — 12 [hp_X]/mLAconitum napellus whole — 12 [hp_X]/mLArsenic trioxide — 12 [hp_X]/mLAtropa belladonna — 12 [hp_X]/mLActivated charcoal — 12 [hp_X]/mLCinchona officinalis bark — 12 [hp_X]/mLConium maculatum flowering top — 12 [hp_X]/mLMercuric chloride — 12 [hp_X]/mLPhosphorus — 12 [hp_X]/mLSulfur — 12 [hp_X]/mLTobacco leaf — 12 [hp_X]/mLNitric acid — 12 [hp_X]/mLAmanita muscaria fruiting body — 30 [hp_C]/mLLachesis muta venom — 30 [hp_C]/mLPhysostigma venenosum seed — 30 [hp_C]/mLTubocurarine chloride — 30 [hp_C]/mL
Dosage form
Spray
Route
Oral
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
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)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)Plant Proteins (Chemical structure)Plant Proteins (Chemical structure)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers
Product ID 43857-0613_fcf7b5ae-e015-446d-96aa-c865a9b0b7b2SPL ID fcf7b5ae-e015-446d-96aa-c865a9b0b7b2SPL set ID 3f9bd6c8-6fc9-4af1-8263-ab42f99fba37UNII 1TH8Q20J0U, 2788Z9758H, 597E9BI3Z3, 4VBP01X99F, QBR70R4FBK, 4JS0838828, 3C3Y389JBU, A4KL1HMZ7T, 11E6VI8VEG, 398IYQ16YV, 6EC706HI7F, 33A7VYU29L, 6RV024OAUQ, C88X29Y479, 269XH13919, E4GA8884NN, U0NQ8555JD, S7V92P67HO, WQZ3G9PF0H, 2P3VWU3H10, S003A158SB, Q28R5GF371, 53GH7MZT1R, 27YLU75U4W, 70FD1KFU70, 6YR2608RSU, 411VRN1TV4, DIF093I037, VSW71SS07I, CJV9E9IIOA, 900961Z8VR
Pharmacologic class
Non-Standardized Food Allergenic Extract; Non-Standardized Plant 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

N443857061301 followed by a unit qualifier and the quantity

Package 43857-0613-01. 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 .

Indications (excerpt from the label)

USES: For the temporary relief of numbness, tingling, trembling, paralysis, short of breath, burning eyes.** **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)

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