NDC codes

FDA NDC Directory
Product NDC (as listed)47219-302Labeler and product segments. Claims need a package NDC.
Product NDC at billing width47219-0302Add 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 NDC11-digit (billing)PackageCopy
47219-302-02472190302021 BOTTLE, DISPENSING in 1 BOX (47219-302-02) / 60 mL in 1 BOTTLE, DISPENSINGMarketed from Oct 27, 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)
Plus Relief
Generic name (nonproprietary)
naja naja venom
Active ingredients
Naja naja venom — 6 [hp_X]/mL
Dosage form
Gel
Route
Topical
Labeler
Nutra Pharma CorporationNDC labeler code 47219
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
Identifiers
Product ID 47219-302_42b5508b-ae27-8aaa-e063-6294a90ae812SPL ID 42b5508b-ae27-8aaa-e063-6294a90ae812SPL set ID 94ea13e4-bd9b-45aa-8993-3a0d0769499fUNII 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. Topical products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N447219030202 followed by a unit qualifier and the quantity

Package 47219-0302-02. 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 .

Indications (excerpt from the label)

USE 3-4 TIMES A DAY. Note: It may take several days to induce relief. Use within 90 days of opening. Store at 50° to 80°F.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 47219-302

What is NDC 47219-302?
47219-302 is the product NDC for Plus Relief (naja naja venom), Naja naja venom 6 [hp_X]/mL gel, 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?
Plus Relief (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 Plus Relief?
3 other product NDCs are listed under this name. See all Plus Relief NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Plus Relief NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Plus Reliefnaja naja venomNaja naja venom 6 [hp_X]/mLGelTopicalNutra Pharma Corporation47219-31247219-0312-02
Plus Reliefnaja naja venomNaja naja venom 6 [hp_X]/mLSpray, MeteredOralNutra Pharma Corporation47219-21147219-0211-01

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Plus Relief NDC 47219-302 | National Drug Code | Med-Code