Eucalyptus Globulus NDC 37662-0682

NDC codes

FDA NDC Directory

Product NDC (as listed)37662-0682Labeler and product segments. Claims need a package NDC.

Product NDC at billing width37662-0682Add 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
37662-0682-1	37662068201	200 PELLET in 1 VIAL, GLASS (37662-0682-1)Marketed from Jun 21, 2022
37662-0682-2	37662068202	1200 PELLET in 1 BOTTLE, GLASS (37662-0682-2)Marketed from Jun 21, 2022
37662-0682-3	37662068203	4000 PELLET in 1 BOTTLE, GLASS (37662-0682-3)Marketed from Jun 21, 2022

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): Eucalyptus Globulus
Generic name (nonproprietary): eucalyptus globulus
Active ingredients: Eucalyptus globulus leaf — 12 [hp_C]/1
Dosage form: Pellet
Route: Oral
Labeler: Hahnemann Laboratories, INC.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jun 21, 2022
Listing expires: Dec 31, 2026
Identifiers: Product ID 37662-0682_e1fe022c-d1db-183a-e053-2995a90ae17fSPL ID e1fe022c-d1db-183a-e053-2995a90ae17fSPL set ID e1fe022c-d1da-183a-e053-2995a90ae17fUNII S546YLW6E6

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

N437662068201 followed by a unit qualifier and the quantity

Package 37662-0682-01. 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 Jun 21, 2022.

Full label on DailyMed (opens in a new tab)