F26 PRSVR

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: F26 PRSVR
Generic name: ALLIUM CEPA WHOLE, APIS MELLIFICA, AURUM METALLICUM, BORAGE, BROMUS RAMOSUS, CALIFORNIA WILDROSE WHOLE, ENGLISH ELM ING TWIG, ENGLISH HAWTHRON, ENGLISH OAK, EUROPEAN HORNBEAM, EUROPEAN OLIVE, GENTIANELLA AMARELLA, GORSE, LARIX DECIDUA, LUFFA OPERCULATA, MERCURIUS SOLUBILIS, MULLEIN, NATRUM MURIATICUM, PENSTEMON DAVIDSONII WHOLE, PLATINUM METALLICUM, PULSATILLA VULGARIS, PURPLE LOOSESTRIFE WHOLE, ROSA CHINENSIS, SCOTCH BROOM, SEPIA, WILD MUSTARD, YERBA SANTA, ZINCUM METALLICUM
Manufacturer: Apex Energetics Inc.
Product type: HUMAN OTC DRUG
SPL set ID: beaef254-bf57-df92-e053-2995a90abd65
SPL ID: 0e772402-6cf5-8c75-e063-6294a90a5c45
Version: 2
Effective date: 2024-01-08
Source export date: 2026-09-28
Source partition: 6
Source file: https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:36:55

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		F26 PRSVR	openfda.brand_name
generic name		ALLIUM CEPA WHOLE, APIS MELLIFICA, AURUM METALLICUM, BORAGE, BROMUS RAMOSUS, CALIFORNIA WILDROSE WHOLE, ENGLISH ELM ING TWIG, ENGLISH HAWTHRON, ENGLISH OAK, EUROPEAN HORNBEAM, EUROPEAN OLIVE, GENTIANELLA AMARELLA, GORSE, LARIX DECIDUA, LUFFA OPERCULATA, MERCURIUS SOLUBILIS, MULLEIN, NATRUM MURIATICUM, PENSTEMON DAVIDSONII WHOLE, PLATINUM METALLICUM, PULSATILLA VULGARIS, PURPLE LOOSESTRIFE WHOLE, ROSA CHINENSIS, SCOTCH BROOM, SEPIA, WILD MUSTARD, YERBA SANTA, ZINCUM METALLICUM	openfda.generic_name
manufacturer name		Apex Energetics Inc.	openfda.manufacturer_name
ndc	package	63479-0626-1	openfda.package_ndc
ndc	product	63479-0626	openfda.product_ndc
ndc11	package	63479062601	derived:openfda.package_ndc
spl id		0e772402-6cf5-8c75-e063-6294a90a5c45	id
spl set id		beaef254-bf57-df92-e053-2995a90abd65	set_id
unii		205JZ3JIKD	openfda.unii
unii		8K9DCX606Z	openfda.unii
unii		9UMZ642257	openfda.unii
unii		8P2VLG2456	openfda.unii
unii		324Y4038G2	openfda.unii
unii		HKE3DK7994	openfda.unii
unii		N7FC535Q3R	openfda.unii
unii		QDL83WN8C2	openfda.unii
unii		ZKH2SOY1AR	openfda.unii
unii		QH060TH2D2	openfda.unii
unii		07YL55QKZ9	openfda.unii
unii		398DBS1PXN	openfda.unii
unii		H14X4P9EKJ	openfda.unii
unii		451W47IQ8X	openfda.unii
unii		79Y1949PYO	openfda.unii
unii		C4MO6809HU	openfda.unii
unii		WWX61E1ZAK	openfda.unii
unii		E9O9E4Q192	openfda.unii
unii		ML644HED2V	openfda.unii
unii		J3O020I532	openfda.unii
unii		NT52AMP29J	openfda.unii
unii		7S82P3R43Z	openfda.unii
unii		498M34P1VZ	openfda.unii
unii		7X23S1OW1N	openfda.unii
unii		J41CSQ7QDS	openfda.unii
unii		I76KB35JEV	openfda.unii
unii		0W9O574LE8	openfda.unii
unii		49DFR088MY	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 eexhaustion, lack of endurance, apathy, easily discouraged, 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.