NDC codes

FDA NDC Directory
Product NDC (as listed)58048-0005Labeler and product segments. Claims need a package NDC.
Product NDC at billing width58048-0005Add 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
58048-0005-1580480005015804800050160 mL in 1 BOTTLE, DROPPER (58048-0005-1)Marketed from Mar 17, 2020

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)
Lyme and Co-Infection Nosode
Generic name (nonproprietary)
angelica archangelica, kali muriaticum, yucca filamentosa, cartilago suis, phytolacca decandra, hydrastis canadensis, rhus tox, causticum, magnesia phosphorica, manganum metallicum, oxalicum acidum, arnica montana, babesia microti, borrelia burgdorferi nosode, latrodectus mactans, citricum acidum, cytomegalovirus nosode, rickettsia nosode (rickettsia prowazekii), chlamydia trachomatis, ledum palustre
Active ingredients
Angelica archangelica root — 2 [hp_X]/mLPotassium chloride — 3 [hp_X]/mLYucca filamentosa — 3 [hp_X]/mLSus scrofa cartilage — 4 [hp_X]/mLPhytolacca americana root — 4 [hp_X]/mLGoldenseal — 5 [hp_X]/mLToxicodendron pubescens leaf — 6 [hp_X]/mLCausticum — 6 [hp_X]/mLMagnesium phosphate, Dibasic trihydrate — 8 [hp_X]/mLManganese — 8 [hp_X]/mLOxalic acid — 8 [hp_X]/mLArnica montana — 8 [hp_X]/mLBabesia microti — 12 [hp_X]/mLBorrelia burgdorferi — 12 [hp_X]/mLLatrodectus mactans — 12 [hp_X]/mLAnhydrous citric acid — 6 [hp_C]/mLHuman herpesvirus 5 — 6 [hp_C]/mLRickettsia prowazekii — 8 [hp_C]/mLChlamydia trachomatis — 12 [hp_C]/mLLedum palustre twig — 30 [hp_C]/mL
Dosage form
Liquid
Route
Oral
Labeler
Bhp Holdings, Inc.NDC labeler code 58048
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Marketing end
Other FDA classes
Acidifying Activity (Mechanism)Calcium Chelating Activity (Mechanism)Decreased Coagulation Factor Activity (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Small Intestine Fluid/Electrolyte Absorption (Physiologic effect)Magnesium Ion Exchange Activity (Mechanism)Osmotic Activity (Mechanism)Osmotic Activity (Mechanism)Potassium Compounds (Chemical structure)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
Identifiers
Product ID 58048-0005_88e0c163-99e8-45bb-8911-8d29370dd909SPL ID 88e0c163-99e8-45bb-8911-8d29370dd909SPL set ID f6186157-256f-4454-b122-f7665e3286f4UNII DTN01M69SN, 660YQ98I10, T6VR38UJ9I, 73ECW5WG2F, 11E6VI8VEG, ZW3Z11D0JV, 6IO182RP7A, DD5FO1WKFU, HF539G9L3Q, 42Z2K6ZL8P, 9E7R5L6H31, O80TY208ZW, 1948X6KEG3, 0J8NV9V5Q8, XJJ7QA858R, XF417D3PSL, 7COI029E6K, TVS414L9M5, T6NI39QU44, 877L01IZ0P
Pharmacologic class
Anti-coagulant; Calculi Dissolution Agent; Osmotic Laxative; Potassium Salt

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

N458048000501 followed by a unit qualifier and the quantity

Package 58048-0005-01. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

About NDC 58048-0005

What is NDC 58048-0005?
58048-0005 is the product NDC for Lyme and Co-Infection Nosode, Angelica archangelica root 2 [hp_X]/mL + 19 more ingredients liquid, listed with the FDA by Bhp Holdings, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Lyme and Co-Infection Nosode (Angelica Archangelica, Kali Muriaticum, Yucca Filamentosa, Cartilago Suis, Phytolacca Decandra, Hydrastis Canadensis, Rhus Tox, Causticum, Magnesia Phosphorica, Manganum Metallicum, Oxalicum Acidum, Arnica Montana, Babesia Microti, Borrelia Burgdorferi Nosode, Latrodectus Mactans, Citricum Acidum, Cytomegalovirus Nosode, Rickettsia Nosode (rickettsia prowazekii), Chlamydia Trachomatis, Ledum Palustre).
What is the active ingredient?
Angelica archangelica root, Potassium chloride, Yucca filamentosa, Sus scrofa cartilage, Phytolacca americana root, Goldenseal, Toxicodendron pubescens leaf, Causticum, Magnesium phosphate, Dibasic trihydrate, Manganese, Oxalic acid, Arnica montana, Babesia microti, Borrelia burgdorferi, Latrodectus mactans, Anhydrous citric acid, Human herpesvirus 5, Rickettsia prowazekii, Chlamydia trachomatis, Ledum palustre twig.
Who is the labeler?
Bhp Holdings, Inc., NDC labeler code 58048. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Lyme and Co-Infection Nosode?
None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

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