Alpha Cf NDC 68466-3398

NDC codes

FDA NDC Directory

Product NDC (as listed)68466-3398Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68466-3398Add 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
68466-3398-1	68466339801	1 BOTTLE, GLASS in 1 BOX (68466-3398-1) / 120 TABLET in 1 BOTTLE, GLASSMarketed from Apr 1, 2017

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): Alpha Cf
Generic name (nonproprietary): aconitum napellus, bryonia alba root, eucalyptus globulus leaf, eupatorium perfoliatum flowering top, gelsemium sempervirens root, ipecac, phosphorus
Active ingredients: Aconitum napellus — 4 [hp_X]/1Bryonia alba root — 4 [hp_X]/1Eupatorium perfoliatum flowering top — 6 [hp_X]/1Gelsemium sempervirens root — 4 [hp_X]/1Ipecac — 3 [hp_X]/1Eucalyptus globulus leaf — 2 [hp_X]/1Phosphorus — 6 [hp_X]/1
Dosage form: Tablet
Route: Sublingual, Sublingual, Sublingual
Labeler: Schwabe Mexico, S.A. de C.V.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Apr 1, 2017
Marketing end: Mar 31, 2027
Identifiers: Product ID 68466-3398_508e09f9-a43d-4cd5-9896-9c4eea845c8fSPL ID 508e09f9-a43d-4cd5-9896-9c4eea845c8fSPL set ID 26afa426-eaae-437f-85a7-3bf0ad3d361bUNII U0NQ8555JD, T7J046YI2B, 1W0775VX6E, 639KR60Q1Q, 62I3C8233L, S546YLW6E6, 27YLU75U4WUPC 0308078033983

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

NDC on a medical claim

N468466339801 followed by a unit qualifier and the quantity

Package 68466-3398-01. 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 May 3, 2022.

Indications (excerpt from the label)

Indication & Usage Uses: Temporarily relieves these symptoms: fever, chills, sneezing, stuffed-up nose, runny nose, coughing, sore throat, headache, minor aches and pains.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)