Renotox NDC 43857-0634

NDC codes

FDA NDC Directory

Product NDC (as listed)43857-0634Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43857-0634Add 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
43857-0634-1	43857063401	60 mL in 1 BOTTLE, DROPPER (43857-0634-1)Marketed from Nov 16, 2023

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): Renotox
Generic name (nonproprietary): triticum aestivum, asparagus officinalis, berberis vulgaris, echinacea (angustifolia), kali muriaticum, petroselinum sativum, sabal serrulata, solidago virgaurea, taraxacum officinale, uva-ursi, barosma (betulina), eupatorium purpureum, kidney (suis), bryonia (alba), mercurius corrosivus, aluminum metallicum, antimonium crudum, argentum metallicum, arsenicum album, aurum metallicum, baryta carbonica, beryllium metallicum, bismuthum metallicum, boron, bromium, cadmium metallicum, cerium metallicum,
Active ingredients: Triticum aestivum whole — 1 [hp_X]/mLAsparagus — 3 [hp_X]/mLBerberis vulgaris root bark — 3 [hp_X]/mLEchinacea angustifolia whole — 3 [hp_X]/mLPotassium chloride — 3 [hp_X]/mLPetroselinum crispum whole — 3 [hp_X]/mLSaw palmetto — 3 [hp_X]/mLSolidago virgaurea flowering top — 3 [hp_X]/mLTaraxacum officinale — 3 [hp_X]/mLArctostaphylos uva-ursi leaf — 3 [hp_X]/mLAgathosma betulina leaf — 5 [hp_X]/mLEutrochium purpureum root — 6 [hp_X]/mLPork kidney — 8 [hp_X]/mLBryonia alba root — 12 [hp_X]/mLMercuric chloride — 12 [hp_X]/mLAluminum — 12 [hp_X]/mLAntimony trisulfide — 12 [hp_X]/mLSilver — 12 [hp_X]/mLArsenic trioxide — 12 [hp_X]/mLGold — 12 [hp_X]/mLBarium carbonate — 12 [hp_X]/mLBeryllium — 12 [hp_X]/mLBismuth — 12 [hp_X]/mLBoron — 12 [hp_X]/mLBromine — 12 [hp_X]/mLCadmium — 12 [hp_X]/mLCerium — 12 [hp_X]/mLCesium chloride — 12 [hp_X]/mLChromium — 12 [hp_X]/mLCobalt — 12 [hp_X]/mLCopper — 12 [hp_X]/mLDysprosium — 12 [hp_X]/mLErbium — 12 [hp_X]/mLEuropium — 12 [hp_X]/mLIron — 12 [hp_X]/mLGadolinium — 12 [hp_X]/mLGermanium sesquioxide — 12 [hp_X]/mLHolmium — 12 [hp_X]/mLIndium — 12 [hp_X]/mLLithium carbonate — 12 [hp_X]/mLMagnesium — 12 [hp_X]/mLManganese — 12 [hp_X]/mLMercurius solubilis — 12 [hp_X]/mLMolybdenum — 12 [hp_X]/mLNeodymium oxide — 12 [hp_X]/mLNickel — 12 [hp_X]/mLOsmium — 12 [hp_X]/mLPalladium — 12 [hp_X]/mLPlatinum — 12 [hp_X]/mLLead — 12 [hp_X]/mLPraseodymium — 12 [hp_X]/mLRhodium — 12 [hp_X]/mLRubidium nitrite — 12 [hp_X]/mLSamarium — 12 [hp_X]/mLSelenium — 12 [hp_X]/mLTin — 12 [hp_X]/mLStrontium carbonate — 12 [hp_X]/mLTerbium — 12 [hp_X]/mLThallium — 12 [hp_X]/mLUranyl nitrate hexahydrate — 12 [hp_X]/mLVanadium — 12 [hp_X]/mLYtterbium oxide — 12 [hp_X]/mLZinc — 12 [hp_X]/mLInfluenza a virus a/victoria/2570/2019 ivr-215 (H1n1) antigen (Uv, Formaldehyde inactivated) — 30 [hp_X]/mLInfluenza a virus a/darwin/9/2021 ivr-228 (H3n2) antigen (Uv, Formaldehyde inactivated) — 30 [hp_X]/mLInfluenza b virus b/austria/1359417/2021 bvr-26 antigen (Uv, Formaldehyde inactivated) — 30 [hp_X]/mLInfluenza b virus b/phuket/3073/2013 antigen (Uv, Formaldehyde inactivated) — 30 [hp_X]/mLMeasles virus — 30 [hp_X]/mLBotulinum toxin type a — 30 [hp_X]/mLEscherichia coli — 30 [hp_X]/mLProteus vulgaris — 30 [hp_X]/mLPseudomonas aeruginosa — 30 [hp_X]/mLProteus morganii — 30 [hp_X]/mLSalmonella enterica enterica serovar typhi — 33 [hp_X]/mLLanthanum — 14 [hp_C]/mLClostridium perfringens — 19 [hp_C]/mLHuman herpesvirus 4 — 30 [hp_C]/mLNiobium — 30 [hp_C]/mLPoliovirus — 30 [hp_C]/mLTantalum — 30 [hp_C]/mL
Dosage form: Liquid
Route: Oral
Labeler: BioActive Nutritional, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Nov 16, 2023
Marketing end: Sep 28, 2028
Other FDA classes: Acetylcholine Release Inhibitors (Mechanism)Allergens (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)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)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Inhibit Ovum Fertilization (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Neuromuscular Blockade (Physiologic effect)Osmotic Activity (Mechanism)Potassium Compounds (Chemical structure)Vegetable Proteins (Chemical structure)
Identifiers: Product ID 43857-0634_6d85d243-0883-4fc7-bc05-87baa26df8e2SPL ID 6d85d243-0883-4fc7-bc05-87baa26df8e2SPL set ID f2b9cc0d-e146-47f7-b1b8-3e4d1cf6d0e9UNII 3C3Y389JBU, Z1EJP3037Z, 1TH8Q20J0U, VB06AV5US8, 660YQ98I10, 1WZA4Y92EX, J7WWH9M8QS, 5405K23S50, 39981FM375, 3M5V3D1X36, 369DDH39Z0, 0VYG5PVN5Q, X7BCI5P86H, T7J046YI2B, 53GH7MZT1R, CPD4NFA903, F79059A38U, 3M4G523W1G, S7V92P67HO, 79Y1949PYO, 6P669D8HQ8, OW5102UV6N, U015TT5I8H, N9E3X5056Q, SBV4XY874G, 00BH33GNGH, 30K4522N6T, GNR9HML8BA, 0R0008Q3JB, 3G0H8C9362, 789U1901C5, 1D4N45714Q, 77B218D3YE, 444W947O8O, E1UOL152H7, AU0V1LM3JT, 96WE91N25T, W1XX32SQN1, 045A6V3VFX, 2BMD2GNA4V, I38ZP9992A, 42Z2K6ZL8P, 324Y4038G2, 81AH48963U, AYT3H319PN, 7OV03QG267, 2E7M255OPY, 5TWQ1V240M, 49DFR088MY, 2P299V784P, NKN7EZA750, DMK383DSAC, 93722E7JA1, 42OD65L39F, H6241UJ22B, 387GMG9FH5, 41YPU4MMCA, 06SSF7P179, AD84R52XLF, 3V057702FY, 00J9J9XKDE, T66CZ53RP4, J41CSQ7QDS, 34C49NV47P, P483J7GX6D, TBV2PPG6EF, H2198F8ZNA, HT3R7C012Q, E211KPY694, 514B9K0L10, 11T9HCO30O, Y793W5V55N, 56X6LID5ZY, 760T5R8B3O, 6I3K30563S, OVP6XX033E, 2A26YW7PNX, 05175J654G, FZJ641678T, 6424HBN274
Pharmacologic class: Acetylcholine Release Inhibitor; Copper-containing Intrauterine Device; Mood Stabilizer; Neuromuscular Blocker; Non-Standardized Food Allergenic Extract; Osmotic Laxative; Potassium Salt; Standardized Chemical Allergen

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

N443857063401 followed by a unit qualifier and the quantity

Package 43857-0634-01. 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 Mar 20, 2025.

Indications (excerpt from the label)

INDICATIONS: For temporary relief of pain in the abdomen extending around to the back, pain in the thighs and loins on urinating and frequent urination.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)