What is NDC 55926-0025?

55926-0025 is the product NDC for emuaidMAX (silver), Silver 10 [hp_X]/100mL ointment, listed with the FDA by Speer Laboratories, LLC. It has 2 package NDCs, shown above in 10- and 11-digit form.

Speer Laboratories, LLC, NDC labeler code 55926. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for emuaidMAX?

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.

emuaidMAX NDC 55926-0025 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)55926-0025Labeler and product segments. Claims need a package NDC.

Product NDC at billing width55926-0025Add 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
55926-0025-2	55926002502	59 mL in 1 BOTTLE (55926-0025-2)Marketed from Jan 22, 2014
55926-0025-3	55926002503	10 mL in 1 TUBE (55926-0025-3)Marketed from Oct 2, 2023

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): emuaidMAX
Generic name (nonproprietary): silver
Active ingredients: Silver — 10 [hp_X]/100mL
Dosage form: Ointment
Route: Topical
Labeler: Speer Laboratories, LLCNDC labeler code 55926
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jan 22, 2014
Listing expires: Dec 31, 2026
Identifiers: Product ID 55926-0025_589aba60-20c0-429a-a136-1679b17bf014SPL ID 589aba60-20c0-429a-a136-1679b17bf014SPL set ID 31640def-5295-4ebc-a861-3b99521bee73UNII 3M4G523W1G

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

N455926002502 followed by a unit qualifier and the quantity

Package 55926-0025-02. 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 14, 2024.

Indications (excerpt from the label)

Indications for Use For the relief of these symptoms due to minor wounds and burns, bruises, ulcerations, sunburn, razor burn, scrapes, rashes, blisters, bug bites, and skin eruptions from acne, eczema, or minor infection: • burning • stinging • itching • redness • stiffness • minor pain • minor inflammation

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 55926-0025

What is NDC 55926-0025?: 55926-0025 is the product NDC for emuaidMAX (silver), Silver 10 [hp_X]/100mL ointment, listed with the FDA by Speer Laboratories, LLC. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: emuaidMAX (Silver).
What is the active ingredient?: Silver.
Who is the labeler?: Speer Laboratories, LLC, NDC labeler code 55926. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for emuaidMAX?: 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.

emuaidMAX (Silver) NDC 55926-0025