Home FDA labels 0e76f50e-2560-d499-e063-6394a90aa92e F05 SLFSTM 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 F05 SLFSTM
Generic name BULBOUS BUTTERCUP, CENTAURY, CERATOSTIGMA WILLMOTTIANUM, JASMINUM OFFICINALE, LAC CANINUM, LARIX DECIDUA, LYCOPODIUM CLAVATUM, ASIMINA TRILOBA, PRICKLY PEAR, PULSATILLA VULGARIS, ROUNDLEAF MALLOW, SAGUARO, SUNFLOWER, TRUMPET VINE, YELLOW JASMINE
Manufacturer Apex Energetics Inc.
Product type HUMAN OTC DRUG
SPL set ID bca81c91-a949-326f-e053-2995a90a45bb
SPL ID 0e76f50e-2560-d499-e063-6394a90aa92e
Version 2
Effective date 2024-01-08
Source export date 2026-09-28
Source partition 2
Source file https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:15:19 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 · 23 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name F05 SLFSTM openfda.brand_name generic name BULBOUS BUTTERCUP, CENTAURY, CERATOSTIGMA WILLMOTTIANUM, JASMINUM OFFICINALE, LAC CANINUM, LARIX DECIDUA, LYCOPODIUM CLAVATUM, ASIMINA TRILOBA, PRICKLY PEAR, PULSATILLA VULGARIS, ROUNDLEAF MALLOW, SAGUARO, SUNFLOWER, TRUMPET VINE, YELLOW JASMINE openfda.generic_name manufacturer name Apex Energetics Inc. openfda.manufacturer_name ndc package 63479-0605-1 openfda.package_ndc ndc product 63479-0605 openfda.product_ndc ndc11 package 63479060501 derived:openfda.package_ndc spl id 0e76f50e-2560-d499-e063-6394a90aa92e id spl set id bca81c91-a949-326f-e053-2995a90a45bb set_id unii S0QQA41760 openfda.unii unii 9UMZ642257 openfda.unii unii Z54WN9192C openfda.unii unii 9I1JVD2I03 openfda.unii unii 639KR60Q1Q openfda.unii unii G39P120JQT openfda.unii unii 83YSP51SMA openfda.unii unii 06M320D5U9 openfda.unii unii AEQ8NXJ0MB openfda.unii unii B204P54Z1F openfda.unii unii TP69J995TW openfda.unii unii 0Q8K841432 openfda.unii unii BKJ0J3D1BP openfda.unii unii I76KB35JEV openfda.unii unii C88X29Y479 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 fatigue, loss of confidence, low-spiritedness, fear, nausea, apprehension, insomnia, 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.