B01 ACUTE RESCUE

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: B01 ACUTE RESCUE
Generic name: ACONITUM NAPELLUS, APIS MELLIFICA, ARNICA MONTANA, ARSENICUM ALBUM, BELLADONNA, BELLIS PERENNIS, BRYONIA ALBA, CALENDULA OFFICINALIS, CHAMOMILLA, CHERRY PLUM, CLEMATIS, COLOCYNTHIS, DULCAMARA, ECHINACEA ANGUSTIFOLIA, ECHINACEA PURPUREA, EUPATORIUM PERFOLIATUM, FERRUM PHOSPHORICUM, HAMAMELIS VIRGINIANA, HISTAMINUM, HYPERICUM PERFORATUM, IMPATIENS, MILLEFOLIUM, RHUS TOXICODENDRON, ROCK ROSE, STAR OF BETHLEHEM, SULPHUR, SYMPHYTUM OFFICINALE, VERATRUM ALBUM
Manufacturer: Apex Energetics Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 4ce96ca9-8964-4b60-9d99-bf01d3d1cb43
SPL ID: 0e76a879-b2c6-dcc6-e063-6294a90ac60e
Version: 4
Effective date: 2024-01-08
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
SUBLINGUAL

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 · 36 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		B01 ACUTE RESCUE	openfda.brand_name
generic name		ACONITUM NAPELLUS, APIS MELLIFICA, ARNICA MONTANA, ARSENICUM ALBUM, BELLADONNA, BELLIS PERENNIS, BRYONIA ALBA, CALENDULA OFFICINALIS, CHAMOMILLA, CHERRY PLUM, CLEMATIS, COLOCYNTHIS, DULCAMARA, ECHINACEA ANGUSTIFOLIA, ECHINACEA PURPUREA, EUPATORIUM PERFOLIATUM, FERRUM PHOSPHORICUM, HAMAMELIS VIRGINIANA, HISTAMINUM, HYPERICUM PERFORATUM, IMPATIENS, MILLEFOLIUM, RHUS TOXICODENDRON, ROCK ROSE, STAR OF BETHLEHEM, SULPHUR, SYMPHYTUM OFFICINALE, VERATRUM ALBUM	openfda.generic_name
manufacturer name		Apex Energetics Inc.	openfda.manufacturer_name
ndc	package	63479-0201-1	openfda.package_ndc
ndc	product	63479-0201	openfda.product_ndc
ndc11	package	63479020101	derived:openfda.package_ndc
spl id		0e76a879-b2c6-dcc6-e063-6294a90ac60e	id
spl set id		4ce96ca9-8964-4b60-9d99-bf01d3d1cb43	set_id
unii		2FXJ6SW4PK	openfda.unii
unii		0KD7R09EAS	openfda.unii
unii		XK4IUX8MNB	openfda.unii
unii		7SCP4N87CI	openfda.unii
unii		3POA0Q644U	openfda.unii
unii		O80TY208ZW	openfda.unii
unii		G72JA9DHK5	openfda.unii
unii		18E7415PXQ	openfda.unii
unii		2HU33I03UY	openfda.unii
unii		CZD6M4PY4B	openfda.unii
unii		M9VVZ08EKQ	openfda.unii
unii		91GQH8I5F7	openfda.unii
unii		6IO182RP7A	openfda.unii
unii		51BRR32WPP	openfda.unii
unii		S7V92P67HO	openfda.unii
unii		VB06AV5US8	openfda.unii
unii		AJU5O1A5ZV	openfda.unii
unii		WQZ3G9PF0H	openfda.unii
unii		T7J046YI2B	openfda.unii
unii		70FD1KFU70	openfda.unii
unii		QI7G114Y98	openfda.unii
unii		U0NQ8555JD	openfda.unii
unii		1W0775VX6E	openfda.unii
unii		7S82P3R43Z	openfda.unii
unii		G0R4UBI2ZZ	openfda.unii
unii		QNS6W5US1Z	openfda.unii
unii		T7S323PKJS	openfda.unii
unii		23H32AOH17	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. Do not use if clear seal over the cap is broken or missing. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Stop use and ask a doctor if inflammation, pain, common cold/flu, bruises, sore throat, muscle aches, or other symptoms do not improve within 7 days or are accompanied by fever.

Reported adverse events (FAERS/openFDA)#

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