Home FDA labels 72aefe28-0790-4c73-b3e5-4928d1966fd6 Vital Female Sexual Energy 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 Vital Female Sexual Energy
Generic name AGNUS CASTUS, ARNICA MONTANA, AVENA SATIVA, CAULOPHYLLUM THALICTROIDES, CINCHONA OFFICINALIS, DAMIANA, HYPOPHYSIS SUIS, L-ARGININE, NATRUM MURIATICUM, OOPHORINUM SUIS, PHOSPHORICUM ACIDUM, SABAL SERRULATA, SEPIA, THUJA OCCIDENTALIS
Manufacturer Liddell Laboratories, Inc.
Product type HUMAN OTC DRUG
SPL set ID 7b15d6fa-eb04-41d2-8a01-6e7408ccf4d3
SPL ID 72aefe28-0790-4c73-b3e5-4928d1966fd6
Version 1
Effective date 2026-01-30
Source export date 2026-10-12
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/2026-10-12/b25dad4aaef9c88f0e827394a34fbbd1ce7d71422fa46b5d1e123befad498c1d/drug-label-0006-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 01:46:34 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 · 24 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Vital Female Sexual Energy openfda.brand_name generic name AGNUS CASTUS, ARNICA MONTANA, AVENA SATIVA, CAULOPHYLLUM THALICTROIDES, CINCHONA OFFICINALIS, DAMIANA, HYPOPHYSIS SUIS, L-ARGININE, NATRUM MURIATICUM, OOPHORINUM SUIS, PHOSPHORICUM ACIDUM, SABAL SERRULATA, SEPIA, THUJA OCCIDENTALIS openfda.generic_name manufacturer name Liddell Laboratories, Inc. openfda.manufacturer_name ndc package 50845-0285-2 openfda.package_ndc ndc package 50845-0285-1 openfda.package_ndc ndc product 50845-0285 openfda.product_ndc ndc11 package 50845028502 derived:openfda.package_ndc ndc11 package 50845028501 derived:openfda.package_ndc spl id 72aefe28-0790-4c73-b3e5-4928d1966fd6 id spl set id 7b15d6fa-eb04-41d2-8a01-6e7408ccf4d3 set_id unii J7WWH9M8QS openfda.unii unii O80TY208ZW openfda.unii unii JTJ6HH6YEH openfda.unii unii QDL83WN8C2 openfda.unii unii 1NT28V9397 openfda.unii unii 451W47IQ8X openfda.unii unii L0PFEMQ1DT openfda.unii unii S7YTV04R8O openfda.unii unii 433OSF3U8A openfda.unii unii S003A158SB openfda.unii unii MA9CQJ3F7F openfda.unii unii E4GA8884NN openfda.unii unii RQ2CFA7WWJ openfda.unii unii 94ZLA3W45F 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: Do not use if you have ever had an allergic reaction to this product or any of its ingredients. Stop use and ask a doctor if symptoms persist for more than 7 days, worsen, or if new symptoms occur. Keep out of reach of children. In case of overdose, get medical help or call a Poison Control Center right away. If pregnant or breast feeding, ask a health professional before using product. Do not use if TAMER EVIDENT seal around neck of bottle is missing or broken. Store at room temperature.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.