SET 4TE HOMO

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: SET 4TE HOMO
Generic name: 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
Manufacturer: Deseret Biologicals, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: e7b8d75b-f2bc-4013-91e7-bf5bbec11a90
SPL ID: 7f8e28f9-4378-4609-bf21-1ea80f2e06b2
Version: 1
Effective date: 2026-06-25
Source export date: 2026-10-12
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:32:32

Harmonized routes table
Harmonized routes
ORAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 28 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		SET 4TE HOMO	openfda.brand_name
generic name		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	openfda.generic_name
manufacturer name		Deseret Biologicals, Inc.	openfda.manufacturer_name
ndc	package	43742-2552-1	openfda.package_ndc
ndc	product	43742-2552	openfda.product_ndc
ndc11	package	43742255201	derived:openfda.package_ndc
spl id		7f8e28f9-4378-4609-bf21-1ea80f2e06b2	id
spl set id		e7b8d75b-f2bc-4013-91e7-bf5bbec11a90	set_id
unii		BR1SN1JS2W	openfda.unii
unii		02F3473H9O	openfda.unii
unii		C151H8M554	openfda.unii
unii		51FI676N6F	openfda.unii
unii		TLM2976OFR	openfda.unii
unii		91D9GV0Z28	openfda.unii
unii		935E97BOY8	openfda.unii
unii		N94C2U587S	openfda.unii
unii		Q09SXY6BFI	openfda.unii
unii		7L3E358N9L	openfda.unii
unii		91GQH8I5F7	openfda.unii
unii		6IO182RP7A	openfda.unii
unii		7THJ3EG9SY	openfda.unii
unii		SI6O3IW77Z	openfda.unii
unii		AE28F7PNPL	openfda.unii
unii		11T9HCO30O	openfda.unii
unii		T7J046YI2B	openfda.unii
unii		706IDJ14B7	openfda.unii
unii		J41CSQ7QDS	openfda.unii
unii		1Y17CTI5SR	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNINGS: If pregnant or breastfeeding, ask a health professional before use. Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away. Tamper Evident: Sealed for your protection. Do not use if seal is broken or missing.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.