Progenite

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: Progenite
Generic name: AMMONIUM CARBONICUM, BARYTA MURIATICA, BORAX, CAULOPHYLLUM THALICTROIDES, NATRUM CARBONICUM, SABAL SERRULATA, SABINA, SULPHURICUM ACIDUM, THIOSINAMINUM, FOLLICULINUM, TUBA UTERINA SUIS, UTERUS SUIS, HYPOTHALAMUS (SUIS), THYROIDINUM (SUIS), AGNUS CASTUS, CONIUM MACULATUM, GRAPHITES, HYOSCYAMUS NIGER, SEPIA, SELENIUM METALLICUM, X-RAY
Manufacturer: Deseret Biologicals
Product type: HUMAN OTC DRUG
SPL set ID: 6051c9d5-36ef-4bfa-baab-9862c94805fb
SPL ID: c1ecefa2-d637-4d59-a749-4bc66d88fc27
Version: 3
Effective date: 2023-12-12
Source export date: 2026-09-28
Source partition: 14
Source file: https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/db99fd80353afecef4949b48edcaa018be72b966b2360184251eb14df43743f9/drug-label-0014-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:40:16

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 · 29 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Progenite	openfda.brand_name
generic name		AMMONIUM CARBONICUM, BARYTA MURIATICA, BORAX, CAULOPHYLLUM THALICTROIDES, NATRUM CARBONICUM, SABAL SERRULATA, SABINA, SULPHURICUM ACIDUM, THIOSINAMINUM, FOLLICULINUM, TUBA UTERINA SUIS, UTERUS SUIS, HYPOTHALAMUS (SUIS), THYROIDINUM (SUIS), AGNUS CASTUS, CONIUM MACULATUM, GRAPHITES, HYOSCYAMUS NIGER, SEPIA, SELENIUM METALLICUM, X-RAY	openfda.generic_name
manufacturer name		Deseret Biologicals	openfda.manufacturer_name
ndc	package	43742-1170-1	openfda.package_ndc
ndc	product	43742-1170	openfda.product_ndc
ndc11	package	43742117001	derived:openfda.package_ndc
spl id		c1ecefa2-d637-4d59-a749-4bc66d88fc27	id
spl set id		6051c9d5-36ef-4bfa-baab-9862c94805fb	set_id
unii		6RV024OAUQ	openfda.unii
unii		J7WWH9M8QS	openfda.unii
unii		4QQN74LH4O	openfda.unii
unii		Q28R5GF371	openfda.unii
unii		JTJ6HH6YEH	openfda.unii
unii		EL5GJ3U77E	openfda.unii
unii		2595C75F1P	openfda.unii
unii		91MBZ8H3QO	openfda.unii
unii		NJ5VT0FKLJ	openfda.unii
unii		QDL83WN8C2	openfda.unii
unii		2HA12BTZ65	openfda.unii
unii		4WRK2153H3	openfda.unii
unii		2DI9HA706A	openfda.unii
unii		O40UQP6WCF	openfda.unii
unii		6PRJ93602P	openfda.unii
unii		433OSF3U8A	openfda.unii
unii		Z5BEX9K2G1	openfda.unii
unii		45P3261C7T	openfda.unii
unii		706IDJ14B7	openfda.unii
unii		H6241UJ22B	openfda.unii
unii		N6R0856Z79	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: Keep out of reach of children. In case of overdose, contact physician or a Poison Control Center right away. If pregnant or breast-feeding, ask a health professional before use. Tamper seal: "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.