Focus

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: Focus
Generic name: GINKGO BILOBA, ALPHA-KETOGLUTARICUM ACIDUM, IODIUM, PHOSPHORUS, SARCOLACTICUM ACID, SACCHARUM OFFICINALE, ADENOSINUM CYCLOPHOSPHORICUM, CEREBRUM SUIS, HYPOTHALAMUS SUIS, SILICEA, ADRENALINUM, AMBRA GRISEA, CARBONEUM SULPHURATUM, TARENTULA HISPANA, AETHUSA CYNAPIUM, BARYTA CARBONICA, HELLEBORUS NIGER, VERATRUM ALBUM, CANDIDA ALBICANS, HYOSCYAMUS NIGER
Manufacturer: Deseret Biologicals, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: e77857b8-be67-4041-8c8d-9772f17c6d06
SPL ID: c3752548-adc7-4883-a6cb-57428c79628b
Version: 5
Effective date: 2024-09-11
Source export date: 2026-10-12
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/b939c18fdf51df171cf60ce5558819d08ac66bb16bb9991d48cbec91028d783e/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:39:34

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		Focus	openfda.brand_name
generic name		GINKGO BILOBA, ALPHA-KETOGLUTARICUM ACIDUM, IODIUM, PHOSPHORUS, SARCOLACTICUM ACID, SACCHARUM OFFICINALE, ADENOSINUM CYCLOPHOSPHORICUM, CEREBRUM SUIS, HYPOTHALAMUS SUIS, SILICEA, ADRENALINUM, AMBRA GRISEA, CARBONEUM SULPHURATUM, TARENTULA HISPANA, AETHUSA CYNAPIUM, BARYTA CARBONICA, HELLEBORUS NIGER, VERATRUM ALBUM, CANDIDA ALBICANS, HYOSCYAMUS NIGER	openfda.generic_name
manufacturer name		Deseret Biologicals, Inc.	openfda.manufacturer_name
ndc	package	43742-1201-1	openfda.package_ndc
ndc	product	43742-1201	openfda.product_ndc
ndc11	package	43742120101	derived:openfda.package_ndc
spl id		c3752548-adc7-4883-a6cb-57428c79628b	id
spl set id		e77857b8-be67-4041-8c8d-9772f17c6d06	set_id
unii		27YLU75U4W	openfda.unii
unii		8ID597Z82X	openfda.unii
unii		4GB5DQR532	openfda.unii
unii		C151H8M554	openfda.unii
unii		S54S8B99E8	openfda.unii
unii		608DGJ6815	openfda.unii
unii		6P669D8HQ8	openfda.unii
unii		9679TC07X4	openfda.unii
unii		F9S9FFU82N	openfda.unii
unii		ETJ7Z6XBU4	openfda.unii
unii		4D7G21HDBC	openfda.unii
unii		YKH834O4BH	openfda.unii
unii		4WRK2153H3	openfda.unii
unii		XTC0D02P6C	openfda.unii
unii		86M454L2TT	openfda.unii
unii		M6936L953C	openfda.unii
unii		E0399OZS9N	openfda.unii
unii		19FUJ2C58T	openfda.unii
unii		QNS6W5US1Z	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: 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.