United States · FDA National Drug Code directory

Hyperthyroid Drops 2029

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
63083-2029_289f2400-c0ff-4e74-9fc4-e7979e0b8970
Product NDC
63083-2029
Form
LIQUID
Composition / generic term
Hyperthyroid Drops
Labeler
Professional Complementary Health Formulas
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start / end (source format)
19840815
Source listing expiry
20271231

Source-listed ingredients

  • POTASSIUM IODIDE — 2 [hp_X]/59mL
  • LYCOPUS VIRGINICUS WHOLE — 2 [hp_X]/59mL
  • APIS MELLIFERA — 3 [hp_X]/59mL
  • ACTIVATED CHARCOAL — 3 [hp_X]/59mL
  • SPONGIA OFFICINALIS SKELETON, ROASTED — 4 [hp_X]/59mL
  • CONIUM MACULATUM FLOWERING TOP — 6 [hp_X]/59mL
  • PHOSPHORUS — 6 [hp_X]/59mL
  • BOS TAURUS PITUITARY GLAND, POSTERIOR — 6 [hp_X]/59mL
  • LACHESIS MUTA VENOM — 8 [hp_X]/59mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 59 mL in 1 BOTTLE, DROPPER (63083-2029-2) · 63083-2029-2

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 →