NDC codes

FDA NDC Directory
Product NDC (as listed)63083-4019Labeler and product segments. Claims need a package NDC.
Product NDC at billing width63083-4019Add 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
63083-4019-26308340190259 mL in 1 BOTTLE, DROPPER (63083-4019-2)Marketed from Aug 15, 1985

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)
Human Papillomavirus Combination 4019Suffix: 4019
Generic name (nonproprietary)
human papillomavirus combination
Active ingredients
Human adenovirus b serotype 3 — 12 [hp_X]/59mLMusa acuminata whole — 12 [hp_X]/59mLHuman papillomavirus serotype 16 whole — 30 [hp_X]/59mL
Dosage form
Liquid
Route
Oral
Labeler
Professional Complementary Health FormulasNDC labeler code 63083
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
Identifiers
Product ID 63083-4019_715066f7-85c1-4f41-9b6c-96cfa5899aedSPL ID 715066f7-85c1-4f41-9b6c-96cfa5899aedSPL set ID de399089-a0b3-4d43-b1e9-fc361a91095bUNII 740KW2J7GZ, 8O2MBI99WR, 063VBA799E

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

N463083401902 followed by a unit qualifier and the quantity

Package 63083-4019-02. 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)

INDICATIONS For the temporary relief of itching, burning, or irritated skin.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 63083-4019

What is NDC 63083-4019?
63083-4019 is the product NDC for Human Papillomavirus Combination 4019, Human adenovirus b serotype 3 12 [hp_X]/59mL + 2 more ingredients liquid, listed with the FDA by Professional Complementary Health Formulas. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Human Papillomavirus Combination 4019 (Human Papillomavirus Combination).
What is the active ingredient?
Human adenovirus b serotype 3, Musa acuminata whole, Human papillomavirus serotype 16 whole.
Who is the labeler?
Professional Complementary Health Formulas, NDC labeler code 63083. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Human Papillomavirus Combination 4019?
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.

Free account

Keep searching with a free account

You’ve used your 3 free searches for this session. Log in or create a free Med-Code account to keep looking up NDCs, J-codes and drugs.

Create a free accountLog in