Set 4Te Homo NDC 43742-2552

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-2552Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-2552Add the package segment from the table below.

Product information

Brand name (proprietary): Set 4Te Homo
Generic name (nonproprietary): adeps suillus, bryonia (alba), calcarea phosphorica, cholinum, dna, dopamine (hydrochloride), ferrum phosphoricum, folic acid, insulinum (human), leptin, magnesia muriatica, l-methionine, methylcobalamin, proteus (vulgaris), rhus tox, riboflavinum, ruta graveolens, saccharum officinale, thiosinaminum, zincum metallicum
Active ingredients: Lard — 9 [hp_X]/mLBryonia alba root — 9 [hp_X]/mLTribasic calcium phosphate — 9 [hp_X]/mLCholine hydroxide — 9 [hp_X]/mLHerring sperm DNA — 9 [hp_X]/mLDopamine hydrochloride — 9 [hp_X]/mLFerrosoferric phosphate — 9 [hp_X]/mLFolic acid — 9 [hp_X]/mLInsulin human — 9 [hp_X]/mLLeptin human — 9 [hp_X]/mLMagnesium chloride — 9 [hp_X]/mLMethionine — 9 [hp_X]/mLMethylcobalamin — 9 [hp_X]/mLProteus vulgaris — 12 [hp_X]/mLToxicodendron pubescens leaf — 9 [hp_X]/mLRiboflavin — 9 [hp_X]/mLRuta graveolens flowering top — 9 [hp_X]/mLSucrose — 9 [hp_X]/mLAllylthiourea — 9 [hp_X]/mLZinc — 9 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Deseret Biologicals, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jun 25, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Calcium (Chemical structure)Catecholamines (Chemical structure)Divalent (Chemical structure)Increased Coagulation Factor Activity (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Small Intestine Fluid/Electrolyte Absorption (Physiologic effect)Insulin (Chemical structure)Magnesium Ion Exchange Activity (Mechanism)Osmotic Activity (Mechanism)Phosphate Chelating Activity (Mechanism)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
Identifiers: Product ID 43742-2552_7f8e28f9-4378-4609-bf21-1ea80f2e06b2SPL ID 7f8e28f9-4378-4609-bf21-1ea80f2e06b2SPL set ID e7b8d75b-f2bc-4013-91e7-bf5bbec11a90UNII SI6O3IW77Z, T7J046YI2B, 91D9GV0Z28, 7THJ3EG9SY, 51FI676N6F, 7L3E358N9L, 91GQH8I5F7, 935E97BOY8, 1Y17CTI5SR, Q09SXY6BFI, 02F3473H9O, AE28F7PNPL, BR1SN1JS2W, 11T9HCO30O, 6IO182RP7A, TLM2976OFR, N94C2U587S, C151H8M554, 706IDJ14B7, J41CSQ7QDS
Pharmacologic class: Blood Coagulation Factor; Calculi Dissolution Agent; Catecholamine; Insulin; Osmotic Laxative; Phosphate Binder

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match: No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

Product label

Current FDA label (SPL), effective Jun 25, 2026.

Indications (excerpt from the label)

USES: • For the temporary relief of symptoms including: • fat metabolism support • satiety • craving support • glp support • support of epigenetic memory of obesity • dopamine support • mood support • inflammation support • cell support • sugar metabolism support • energy support • liver support These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)