Gout Pain Management NDC 51393-7656

NDC codes

FDA NDC Directory

Product NDC (as listed)51393-7656Labeler and product segments. Claims need a package NDC.

Product NDC at billing width51393-7656Add 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
51393-7656-1	51393765601	11 mL in 1 BOTTLE, DISPENSING (51393-7656-1)Marketed from Feb 15, 2017
51393-7656-3	51393765603	30 mL in 1 BOTTLE, DISPENSING (51393-7656-3)Marketed from Dec 1, 2025
51393-7656-4	51393765604	4 mL in 1 BOTTLE, DISPENSING (51393-7656-4)Marketed from Feb 15, 2017

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): Gout Pain ManagementSuffix: Pain Management
Generic name (nonproprietary): arnica montana, urtica urens, silicon dioxide, and thuja occidentalis leaf
Active ingredients: Arnica montana whole — 30 [hp_C]/1000mLUrtica urens whole — 30 [hp_C]/1000mLSilicon dioxide — 8 [hp_X]/1000mLThuja occidentalis leaf — 12 [hp_X]/1000mL
Dosage form: Solution/ drops
Route: Topical
Labeler: Forces of Nature
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Feb 15, 2017
Listing expires: Dec 31, 2026
Identifiers: Product ID 51393-7656_c5752aa4-40c2-4f35-a13f-d5684ec08969SPL ID c5752aa4-40c2-4f35-a13f-d5684ec08969SPL set ID 9276fe9c-d9a2-4cef-986c-5d7d39f2d6a1UNII O80TY208ZW, IHN2NQ5OF9, ETJ7Z6XBU4, 0T0DQN8786

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

N451393765601 followed by a unit qualifier and the quantity

Package 51393-7656-01. 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 Nov 25, 2025.

Indications (excerpt from the label)

Indications Topical Analgesic: For the temporary relief of minor aches and pains associated with gout.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)