D82 NDC 58264-0083

NDC codes

FDA NDC Directory

Product NDC (as listed)58264-0083Labeler and product segments. Claims need a package NDC.

Product NDC at billing width58264-0083Add 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
58264-0083-1	58264008301	29.57 mL in 1 BOTTLE, DROPPER (58264-0083-1)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): D82
Generic name (nonproprietary): achillea millefolium, arnica montana, hypericum perforatum, horse chestnut, and viscum album whole
Active ingredients: Achillea millefolium — 3 [hp_X]/mLArnica montana — 6 [hp_X]/mLHypericum perforatum — 3 [hp_X]/mLHorse chestnut — 2 [hp_X]/mLViscum album whole — 3 [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
Identifiers: Product ID 58264-0083_2b9ec82d-e5f9-ae16-e063-6394a90a5559SPL ID 2b9ec82d-e5f9-ae16-e063-6394a90a5559SPL set ID 2c24bb97-11be-450a-9cf9-5aadca1e8be1UNII 2FXJ6SW4PK, O80TY208ZW, XK4IUX8MNB, 3C18L6RJAZ, E6839Q6DO1

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

N458264008301 followed by a unit qualifier and the quantity

Package 58264-0083-01. 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 Stress, headache, sweating, rapid pulse, shortness of breath, dizziness, vision disturbances.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)