NDC codes

FDA NDC Directory
Product NDC (as listed)63083-9201Labeler and product segments. Claims need a package NDC.
Product NDC at billing width63083-9201Add 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
63083-9201-16308392010129.5 mL in 1 BOTTLE, DROPPER (63083-9201-1)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)
Aconitum Combination 9201Suffix: 9201
Generic name (nonproprietary)
aconitum combination
Active ingredients
Eucalyptus globulus leaf — 2 [hp_X]/29.5mLAconitum napellus whole — 3 [hp_X]/29.5mLIpecac — 3 [hp_X]/29.5mL
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 63083-9201_7e030a18-d73a-44d4-a2e6-c120d0284074SPL ID 7e030a18-d73a-44d4-a2e6-c120d0284074SPL set ID a9704081-067e-48dd-bcfd-02eddb1cf279UNII S546YLW6E6, U0NQ8555JD, 62I3C8233L

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

N463083920101 followed by a unit qualifier and the quantity

Package 63083-9201-01. 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 .

Indications (excerpt from the label)

INDICATIONS For the temporary relief of congestion, coughing, sore throat, hoarseness, sneezing, acute fever, or minor body aches or pains.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 63083-9201

What is NDC 63083-9201?
63083-9201 is the product NDC for Aconitum Combination 9201 (aconitum combination), Eucalyptus globulus leaf 2 [hp_X]/29.5mL + 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?
Aconitum Combination 9201 (Aconitum Combination).
What is the active ingredient?
Eucalyptus globulus leaf, Aconitum napellus whole, Ipecac.
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 Aconitum Combination 9201?
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.

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