BP Reg

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: BP Reg
Generic name: ALLIUM SATIVUM, ADRENALINUM, ARTERIA SUIS, CORTISONE ACETICUM, THYROIDINUM (SUIS), VENA SUIS, FORMALINUM, KALI CHLORICUM, ALPHA-LIPOICUM ACIDUM, AURUM METALLICUM, CACTUS GRANDIFLORUS, CHOLESTERINUM, COUMARINUM, EPHEDRA VULGARIS, GLONOINUM, LACHESIS MUTUS, RAUWOLFIA SERPENTINA, STRONTIUM CARBONICUM, SULPHUR, VERATRUM ALBUM, PROTEUS (VULGARIS)
Manufacturer: Deseret Biologicals, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: f99833d8-d637-4c63-afe8-25eb2f05de6a
SPL ID: 44080616-63f6-4943-a9ef-b8a0e4a07a82
Version: 3
Effective date: 2024-05-08
Source export date: 2026-10-12
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:14:39

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		BP Reg	openfda.brand_name
generic name		ALLIUM SATIVUM, ADRENALINUM, ARTERIA SUIS, CORTISONE ACETICUM, THYROIDINUM (SUIS), VENA SUIS, FORMALINUM, KALI CHLORICUM, ALPHA-LIPOICUM ACIDUM, AURUM METALLICUM, CACTUS GRANDIFLORUS, CHOLESTERINUM, COUMARINUM, EPHEDRA VULGARIS, GLONOINUM, LACHESIS MUTUS, RAUWOLFIA SERPENTINA, STRONTIUM CARBONICUM, SULPHUR, VERATRUM ALBUM, PROTEUS (VULGARIS)	openfda.generic_name
manufacturer name		Deseret Biologicals, Inc.	openfda.manufacturer_name
ndc	package	43742-1414-1	openfda.package_ndc
ndc	product	43742-1414	openfda.product_ndc
ndc11	package	43742141401	derived:openfda.package_ndc
spl id		44080616-63f6-4943-a9ef-b8a0e4a07a82	id
spl set id		f99833d8-d637-4c63-afe8-25eb2f05de6a	set_id
unii		6RV024OAUQ	openfda.unii
unii		V1V998DC17	openfda.unii
unii		H192N84N1G	openfda.unii
unii		883WKN7W8X	openfda.unii
unii		73Y7P0K73Y	openfda.unii
unii		79Y1949PYO	openfda.unii
unii		YKH834O4BH	openfda.unii
unii		63O327782Q	openfda.unii
unii		H35KS68EE7	openfda.unii
unii		97C5T2UQ7J	openfda.unii
unii		R55VQ87DP3	openfda.unii
unii		11T9HCO30O	openfda.unii
unii		A4VZ22K1WT	openfda.unii
unii		70FD1KFU70	openfda.unii
unii		VSW71SS07I	openfda.unii
unii		G59M7S0WS3	openfda.unii
unii		1HG84L3525	openfda.unii
unii		2510RH3I89	openfda.unii
unii		QNS6W5US1Z	openfda.unii
unii		41YPU4MMCA	openfda.unii
unii		7114SV0MYK	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 breast-feeding, 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.