United States · FDA National Drug Code directory
Parathyropar
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
- 44911-0902_f12512d9-d32e-47cb-ab90-5b8cdb3961ec
- Product NDC
- 44911-0902
- Form
- LIQUID
- Composition / generic term
- Symphytum Officinale, Baryta Carbonica, Calcarea Carbonica, Calcarea Phosphorica, Hekla Lava, Manganum Metallicum, Parathyroid Gland (Bovine), Rhus Tox, Silicea
- Labeler
- Energique, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start / end (source format)
- 20260105
- Source listing expiry
- 20271231
Source-listed ingredients
- COMFREY ROOT — 6 [hp_X]/mL
- BARIUM CARBONATE — 12 [hp_X]/mL
- OYSTER SHELL CALCIUM CARBONATE, CRUDE — 12 [hp_X]/mL
- TRIBASIC CALCIUM PHOSPHATE — 12 [hp_X]/mL
- HEKLA LAVA — 12 [hp_X]/mL
- MANGANESE — 12 [hp_X]/mL
- BOS TAURUS PARATHYROID GLAND — 12 [hp_X]/mL
- TOXICODENDRON PUBESCENS LEAF — 12 [hp_X]/mL
- SILICON DIOXIDE — 12 [hp_X]/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 30 mL in 1 BOTTLE, DROPPER (44911-0902-1) · 44911-0902-1
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 →