DB Foot Pain Relieving NDC 43689-0070

NDC codes

FDA NDC Directory

Product NDC (as listed)43689-0070Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43689-0070Add 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
43689-0070-3	43689007003	85 g in 1 BOTTLE, SPRAY (43689-0070-3)Marketed from Dec 1, 2025

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): DB Foot Pain Relieving
Generic name (nonproprietary): apis mellifica, gelsemium sempervirens, gnaphalium
Active ingredients: Pseudognaphalium luteoalbum leaf — 3 [hp_X]/100gGelsemium sempervirens whole — 6 [hp_X]/100gApis mellifera — 3 [hp_X]/100g
Dosage form: Spray
Route: Topical
Labeler: The Magni Company
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Dec 1, 2025
Listing expires: Dec 31, 2027
Other FDA classes: Allergens (Chemical structure)Bee Venoms (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)
Identifiers: Product ID 43689-0070_52b905b2-0678-bf51-e063-6294a90a3d11SPL ID 52b905b2-0678-bf51-e063-6294a90a3d11SPL set ID 2e47343c-a64a-4c75-a7ec-f7eedf7518eaUNII BGI20Z6M57, R0519OZO3K, 7S82P3R43Z
Pharmacologic class: Standardized Insect Venom Allergenic Extract

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

N443689007003 followed by a unit qualifier and the quantity

Package 43689-0070-03. 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 May 26, 2026.

Indications (excerpt from the label)

Use: Temporarily Relieves Foot Pain

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)