Rhus tox (toxicodendron pubescens leaf) NDC 0220-4400

NDC codes

FDA NDC Directory

Product NDC (as listed)0220-4400Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00220-4400Add 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
0220-4400-41	00220440041	30 [hp_C] in 1 TUBE (0220-4400-41)Marketed from Mar 3, 1983
0220-4400-43	00220440043	3 TUBE in 1 BOX (0220-4400-43) / 30 [hp_C] in 1 TUBEMarketed from Sep 1, 2020

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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): Rhus tox
Generic name (nonproprietary): toxicodendron pubescens leaf
Active ingredients: Toxicodendron pubescens leaf — 30 [hp_C]/30[hp_C]
Dosage form: Pellet
Route: Oral
Labeler: Boiron
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Mar 3, 1983
Listing expires: Dec 31, 2026
Identifiers: Product ID 0220-4400_fe916773-3d0c-6242-e053-6394a90ab4d7SPL ID fe916773-3d0c-6242-e053-6394a90ab4d7SPL set ID 86abfdc2-d556-4adb-e053-2991aa0a54b1UNII 6IO182RP7A

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

N400220440041 followed by a unit qualifier and the quantity

Package 00220-4400-41. 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 20, 2023.

Indications (excerpt from the label)

Tube - Joint Pain Improved By Motion* Box - temporarily relieves symptoms of joint pain including: swollen joints, pain improved by motion, muscle aches, stiffness, pain aggravated by exposure to cold and damp weather

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)