H-Gout Formula NDC 61077-135

NDC codes

FDA NDC Directory

Product NDC (as listed)61077-135Labeler and product segments. Claims need a package NDC.

Product NDC at billing width61077-0135Add 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
61077-135-11	61077013511	11 mL in 1 BOTTLE, DROPPER (61077-135-11)Marketed from Oct 29, 2014
61077-135-33	61077013533	33 mL in 1 BOTTLE, DROPPER (61077-135-33)Marketed from Oct 29, 2014

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): H-Gout Formula
Generic name (nonproprietary): arnica montana, rhododendron
Active ingredients: Arnica montana — 12 [hp_C]/11mLRhododendron aureum leaf — 6 [hp_C]/11mL
Dosage form: Oil
Route: Topical
Labeler: Healing Natural Oils LLC
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Oct 29, 2014
Listing expires: Dec 31, 2026
Identifiers: Product ID 61077-135_2906c142-d151-b339-e063-6294a90a4b76SPL ID 2906c142-d151-b339-e063-6294a90a4b76SPL set ID 10b7b1ed-e5d4-4157-a7f7-65a8b2876245UNII O80TY208ZW, IV92NQJ73U

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

N461077013511 followed by a unit qualifier and the quantity

Package 61077-0135-11. 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 Dec 11, 2024.

Indications (excerpt from the label)

Indications: For the temporary relief of gout symptoms.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)