United States · FDA National Drug Code directory

ALPHA CF

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference: 68466-3398_508e09f9-a43d-4cd5-9896-9c4eea845c8f
Product NDC: 68466-3398
Form: TABLET
Composition / generic term: ACONITUM NAPELLUS, BRYONIA ALBA ROOT, EUCALYPTUS GLOBULUS LEAF, EUPATORIUM PERFOLIATUM FLOWERING TOP, GELSEMIUM SEMPERVIRENS ROOT, IPECAC, PHOSPHORUS
Labeler: Schwabe Mexico, S.A. de C.V.
Marketing category: UNAPPROVED HOMEOPATHIC
Marketing start / end (source format): 20170401 / 20270331

Source-listed ingredients

ACONITUM NAPELLUS — 4 [hp_X]/1
BRYONIA ALBA ROOT — 4 [hp_X]/1
EUPATORIUM PERFOLIATUM FLOWERING TOP — 6 [hp_X]/1
GELSEMIUM SEMPERVIRENS ROOT — 4 [hp_X]/1
IPECAC — 3 [hp_X]/1
EUCALYPTUS GLOBULUS LEAF — 2 [hp_X]/1
PHOSPHORUS — 6 [hp_X]/1

These values do not establish equivalence or a dose recommendation.

Packages

1 BOTTLE, GLASS in 1 BOX (68466-3398-1) / 120 TABLET in 1 BOTTLE, GLASS · 68466-3398-1

Source and coverage

Open FDA National Drug Code directory →

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

Browse United States records →