Hyperactivity-Mental 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: Hyperactivity-Mental Focus
Generic name: ADRENALINUM, ACONITUM NAP., ARG. NIT., ARSENICUM ALB., BAPTISIA, CHAMOMILLA, CYPRIPEDIUM, DIGITALIS, GELSEMIUM, HUMULUS, IGNATIA, IMPATIENS GLANDULIFERA FLOS, IODIUM, LACHESIS, LYCOPODIUM, NAT. MUR., NUX VOM., SCUTELLARIA LATERIFLORA, STAPHYSAG., STRAMONIUM, THERIDION, ECHINACEA, GINGKO, HYPERICUM, PASSIFLORA
Manufacturer: Newton Laboratories, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: fecece1f-22bc-21dc-e053-6294a90ad0c3
SPL ID: fececb65-2bc7-1954-e053-6394a90ad851
Version: 1
Effective date: 2023-06-23
Source export date: 2026-09-28
Source partition: 10
Source file: https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:07:17

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 · 33 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Hyperactivity-Mental Focus	openfda.brand_name
generic name		ADRENALINUM, ACONITUM NAP., ARG. NIT., ARSENICUM ALB., BAPTISIA, CHAMOMILLA, CYPRIPEDIUM, DIGITALIS, GELSEMIUM, HUMULUS, IGNATIA, IMPATIENS GLANDULIFERA FLOS, IODIUM, LACHESIS, LYCOPODIUM, NAT. MUR., NUX VOM., SCUTELLARIA LATERIFLORA, STAPHYSAG., STRAMONIUM, THERIDION, ECHINACEA, GINGKO, HYPERICUM, PASSIFLORA	openfda.generic_name
manufacturer name		Newton Laboratories, Inc.	openfda.manufacturer_name
ndc	package	55714-2580-1	openfda.package_ndc
ndc	product	55714-2580	openfda.product_ndc
ndc11	package	55714258001	derived:openfda.package_ndc
spl id		fececb65-2bc7-1954-e053-6394a90ad851	id
spl set id		fecece1f-22bc-21dc-e053-6294a90ad0c3	set_id
unii		XK4IUX8MNB	openfda.unii
unii		269XH13919	openfda.unii
unii		00543AP1JV	openfda.unii
unii		639KR60Q1Q	openfda.unii
unii		9679TC07X4	openfda.unii
unii		95IT3W8JZE	openfda.unii
unii		451W47IQ8X	openfda.unii
unii		1NM3M2487K	openfda.unii
unii		YKH834O4BH	openfda.unii
unii		S7V92P67HO	openfda.unii
unii		AJU5O1A5ZV	openfda.unii
unii		4N9P6CC1DX	openfda.unii
unii		7BP4DH5PDC	openfda.unii
unii		VSW71SS07I	openfda.unii
unii		U0NQ8555JD	openfda.unii
unii		G6W4F0V8Z3	openfda.unii
unii		01G73H6H83	openfda.unii
unii		19FUJ2C58T	openfda.unii
unii		5EF0HWI5WU	openfda.unii
unii		9Z8D3HEM8L	openfda.unii
unii		CLF5YFS11O	openfda.unii
unii		F1T8QT9U8B	openfda.unii
unii		G0R4UBI2ZZ	openfda.unii
unii		C88X29Y479	openfda.unii
unii		21Y9GZ1LZA	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 SECTION WARNINGS: Keep out of reach of children . Do not use if tamper-evident seal is broken or missing. If symptoms worsen or persist for more than a few days, consult a doctor. If pregnant or breast-feeding, ask a doctor before use.

Reported adverse events (FAERS/openFDA)#

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