What is NDC 51393-7656?

51393-7656 is the product NDC for Gout Pain Management, Arnica montana whole 30 [hp_C]/1000mL + 3 more ingredients solution/ drops, listed with the FDA by Forces of Nature. It has 3 package NDCs, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Gout Pain Management (Arnica Montana, Urtica Urens, Silicon Dioxide, and Thuja Occidentalis Leaf).

What is the active ingredient?

Arnica montana whole, Urtica urens whole, Silicon dioxide, Thuja occidentalis leaf.

Forces of Nature, NDC labeler code 51393. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Gout Pain Management?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

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	5139376560151393765601	11 mL in 1 BOTTLE, DISPENSING (51393-7656-1)Marketed from Feb 15, 2017
51393-7656-3	5139376560351393765603	30 mL in 1 BOTTLE, DISPENSING (51393-7656-3)Marketed from Dec 1, 2025
51393-7656-4	5139376560451393765604	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 NatureNDC labeler code 51393
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)

About NDC 51393-7656

What is NDC 51393-7656?: 51393-7656 is the product NDC for Gout Pain Management, Arnica montana whole 30 [hp_C]/1000mL + 3 more ingredients solution/ drops, listed with the FDA by Forces of Nature. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Gout Pain Management (Arnica Montana, Urtica Urens, Silicon Dioxide, and Thuja Occidentalis Leaf).
What is the active ingredient?: Arnica montana whole, Urtica urens whole, Silicon dioxide, Thuja occidentalis leaf.
Who is the labeler?: Forces of Nature, NDC labeler code 51393. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Gout Pain Management?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.