What is NDC 47219-215?

47219-215 is the product NDC for Ultimate Pain Block (naja naja venom), Naja naja venom 4 [hp_X]/mL spray, metered, listed with the FDA by Nutra Pharma Corporation. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Ultimate Pain Block (Naja naja venom).

Nutra Pharma Corporation, NDC labeler code 47219. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Ultimate Pain Block?

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.

Ultimate Pain Block NDC 47219-215 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)47219-215Labeler and product segments. Claims need a package NDC.

Product NDC at billing width47219-0215Add 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
47219-215-01	47219021501	1 BOTTLE, SPRAY in 1 BOX (47219-215-01) / 60 mL in 1 BOTTLE, SPRAYMarketed from Oct 29, 2025

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): Ultimate Pain Block
Generic name (nonproprietary): naja naja venom
Active ingredients: Naja naja venom — 4 [hp_X]/mL
Dosage form: Spray, Metered
Route: Oral
Labeler: Nutra Pharma CorporationNDC labeler code 47219
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Oct 29, 2025
Listing expires: Dec 31, 2026
Identifiers: Product ID 47219-215_42c7a251-c012-8b2e-e063-6294a90a43d6SPL ID 42c7a251-c012-8b2e-e063-6294a90a43d6SPL set ID 30a7ab1c-650a-4a8c-95bc-4ab9f2c0cd0fUNII ZZ4AG7L7VM

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. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N447219021501 followed by a unit qualifier and the quantity

Package 47219-0215-01. 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 4, 2025.

Indications (excerpt from the label)

USE SPRAY INITIALLY EVERY 3-4 HOURS. Note: It may take several days to induce relief. Use within 90 days of opening. Store at 50º to 80ºF.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 47219-215

What is NDC 47219-215?: 47219-215 is the product NDC for Ultimate Pain Block (naja naja venom), Naja naja venom 4 [hp_X]/mL spray, metered, listed with the FDA by Nutra Pharma Corporation. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Ultimate Pain Block (Naja naja venom).
What is the active ingredient?: Naja naja venom.
Who is the labeler?: Nutra Pharma Corporation, NDC labeler code 47219. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Ultimate Pain Block?: 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.

Ultimate Pain Block (Naja naja venom) NDC 47219-215