Bestmade Natural Products BM64 NDC 82969-2064

NDC codes

FDA NDC Directory

Product NDC (as listed)82969-2064Labeler and product segments. Claims need a package NDC.

Product NDC at billing width82969-2064Add 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
82969-2064-1	82969206401	200 [hp_C] in 1 BOTTLE, GLASS (82969-2064-1)Marketed from Jan 1, 2015

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): Bestmade Natural Products BM64
Generic name (nonproprietary): chloremphenicol, hypophysis, lobelia erenus, streptomycin, urea
Active ingredients: Urea — 200 [hp_C]/200[hp_C]Chloramphenicol — 200 [hp_C]/200[hp_C]Lobelia erinus — 200 [hp_C]/200[hp_C]Streptomyces griseus — 200 [hp_C]/200[hp_C]Sus scrofa pituitary gland — 200 [hp_C]/200[hp_C]
Dosage form: Liquid
Route: Oral
Labeler: Bestmade Natural Products
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jan 1, 2015
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Amphenicols (EXT)Bacterial Proteins (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)
Identifiers: Product ID 82969-2064_2ceaa0c4-3af3-432f-e063-6294a90af645SPL ID 2ceaa0c4-3af3-432f-e063-6294a90af645SPL set ID 2ceaa0c4-3af2-432f-e063-6294a90af645UNII 8W8T17847W, 66974FR9Q1, K82E711D2W, G0O5980Z7W, L0PFEMQ1DT
Pharmacologic class: Amphenicol-class Antibacterial; Non-Standardized Bacterial 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

N482969206401 followed by a unit qualifier and the quantity

Package 82969-2064-01. 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 Jan 30, 2025.

Indications (excerpt from the label)

Uses Temporarily relieves discomfort due to kidney issues, including occasional frequent urination, foamy urine, headaches, increased blood pressure levels, increased tiredness, itching, lower back discomfort, nausea, loss of appetite, vomiting, need to urinate at night, muscle twitching, and cramps.* *CLAIMS BASED ON TRADITIONAL HOMEOPATHIC PRACTICE, NOT ACCEPTED MEDICAL EVIDENCE, NOT FDA EVALUATED. This product is not intended to diagnose, treat, cure, or prevent any disease.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)