United States · FDA National Drug Code directory

Aletris Combination 9203

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
63083-9203_eb4d236e-99a3-435e-b20b-b13d8b1f5086
Product NDC
63083-9203
Form
LIQUID
Composition / generic term
Aletris Combination
Labeler
Professional Complementary Health Formulas
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start / end (source format)
19840815
Source listing expiry
20271231

Source-listed ingredients

  • ALETRIS FARINOSA ROOT — 4 [hp_X]/29.5mL
  • ANAMIRTA COCCULUS FRUIT — 4 [hp_X]/29.5mL
  • IRON — 6 [hp_X]/29.5mL
  • FERRIC CATION — 6 [hp_X]/29.5mL
  • FERROSOFERRIC PHOSPHATE — 6 [hp_X]/29.5mL
  • FERROUS CATION — 6 [hp_X]/29.5mL
  • CHAMAELIRIUM LUTEUM ROOT — 6 [hp_X]/29.5mL
  • SODIUM CHLORIDE — 6 [hp_X]/29.5mL
  • PICRIC ACID — 6 [hp_X]/29.5mL
  • SEPIA OFFICINALIS JUICE — 6 [hp_X]/29.5mL
  • QUININE ARSENITE — 8 [hp_X]/29.5mL
  • POTASSIUM CARBONATE — 8 [hp_X]/29.5mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 29.5 mL in 1 BOTTLE, DROPPER (63083-9203-1) · 63083-9203-1

Source and coverage

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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.

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