United States · FDA National Drug Code directory

Thyroplus

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: 43742-1010_1bd52e0c-411a-4883-aa1e-0f89719110c8
Product NDC: 43742-1010
Form: LIQUID
Composition / generic term: Fucus Vesiculosus, Spongia Tosta, Phosphoricum Acidum, Hypophysis (Suis), Thyroidinum (Suis), Calcarea Carbonica, Iodium, Iridium Metallicum
Labeler: Deseret Biologicals, Inc.
Marketing category: UNAPPROVED HOMEOPATHIC
Marketing start / end (source format): 20170809
Source listing expiry: 20261231

Source-listed ingredients

FUCUS VESICULOSUS — 3 [hp_X]/mL
SPONGIA OFFICINALIS SKELETON, ROASTED — 4 [hp_X]/mL
PHOSPHORIC ACID — 6 [hp_X]/mL
SUS SCROFA PITUITARY GLAND — 8 [hp_X]/mL
THYROID — 8 [hp_X]/mL
OYSTER SHELL CALCIUM CARBONATE, CRUDE — 12 [hp_X]/mL
IODINE — 12 [hp_X]/mL
IRIDIUM — 12 [hp_X]/mL

These values do not establish equivalence or a dose recommendation.

Packages

30 mL in 1 BOTTLE, DROPPER (43742-1010-1) · 43742-1010-1

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 →