Pain Relief Arnica And Hemp NDC 73002-332

NDC codes

FDA NDC Directory

Product NDC (as listed)73002-332Labeler and product segments. Claims need a package NDC.

Product NDC at billing width73002-0332Add 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
73002-332-02	73002033202	56 mL in 1 BOTTLE (73002-332-02)Marketed from Sep 1, 2020

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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): Pain Relief Arnica And Hemp
Generic name (nonproprietary): arnica (a. montana) tinc, hemp extract (cannabis sativa) 1x
Active ingredients: Arnica montana flower — 70 mg/mLCannabis sativa subsp. Sativa flowering top — 15.7 mg/mL
Dosage form: Lotion
Route: Topical
Labeler: Green Earth Health Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Sep 1, 2020
Marketing end: Sep 30, 2026
Identifiers: Product ID 73002-332_3a88e6e4-1c5d-ddc6-e063-6294a90a7de4SPL ID 3a88e6e4-1c5d-ddc6-e063-6294a90a7de4SPL set ID c0f2fcf6-c54a-4533-8bf9-2ae95a3a57f1UNII OZ0E5Y15PZ, 8X454SZ22D

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

NDC on a medical claim

N473002033202 followed by a unit qualifier and the quantity

Package 73002-0332-02. 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 Jul 22, 2025.

Indications (excerpt from the label)

Indication: Temporarily relieves pain associated with bruises, sore feet, muscle pain and strains

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)