D-33 NDC 58264-0033

NDC codes

FDA NDC Directory

Product NDC (as listed)58264-0033Labeler and product segments. Claims need a package NDC.

Product NDC at billing width58264-0033Add 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
58264-0033-1	58264003301	29.57 mL in 1 BOTTLE, GLASS (58264-0033-1)Marketed from Jan 1, 1990

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): D-33
Generic name (nonproprietary): atropa belladonna, bufo bufo cutaneous gland, copper, anemone pratensis, silicon dioxide, and zinc
Active ingredients: Atropa belladonna — 30 [hp_X]/mLBufo bufo cutaneous gland — 200 [hp_X]/mLCopper — 12 [hp_X]/mLAnemone pratensis — 30 [hp_X]/mLSilicon dioxide — 30 [hp_X]/mLZinc — 12 [hp_X]/mL
Dosage form: Solution
Route: Sublingual
Labeler: DNA Labs, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jan 1, 1990
Listing expires: Dec 31, 2026
Other FDA classes: Copper (Chemical structure)Decreased Embryonic Implantation (Physiologic effect)Decreased Sperm Motility (Physiologic effect)Inhibit Ovum Fertilization (Physiologic effect)
Identifiers: Product ID 58264-0033_2b9eb825-2e83-846c-e063-6394a90a0a7bSPL ID 2b9eb825-2e83-846c-e063-6394a90a0a7bSPL set ID 26f9bf6d-6038-42e8-b8c1-6c94ac4929afUNII WQZ3G9PF0H, Q59QU6N72Q, 789U1901C5, 8E272251DI, ETJ7Z6XBU4, J41CSQ7QDS
Pharmacologic class: Copper-containing Intrauterine Device

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. Sublingual products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N458264003301 followed by a unit qualifier and the quantity

Package 58264-0033-01. 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 13, 2025.

Indications (excerpt from the label)

INDICATIONS Epilepsy, irritations of the nerve.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)