Home FDA labels 7498b0f5-fe09-482d-8a6c-c59066623800 Vital Weight Loss XL 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 Weight Loss XL
Generic name ANTIMONIUM CRUDUM, APIS MELLIFICA, CAPSICUM ANNUUM, FUCUS VESICULOSUS, GALIUM APARINE, GARCINIA CAMBOGIA, HAMAMELIS VIRGINIANA, HEPAR SUIS, HISTAMINUM HYDROCHLORICUM, NUX VOMICA, PANCREAS SUIS, PETROSELINUM SATIVUM, THUJA OCCIDENTALIS, THYROIDINUM SUIS, ZINGIBER OFFICINALE
Manufacturer Liddell Laboratories, Inc.
Product type HUMAN OTC DRUG
SPL set ID fbdf83c5-bc84-485e-8744-01b0bc504138
SPL ID 7498b0f5-fe09-482d-8a6c-c59066623800
Version 6
Effective date 2024-07-01
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 06:07:27 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 · 25 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Vital Weight Loss XL openfda.brand_name generic name ANTIMONIUM CRUDUM, APIS MELLIFICA, CAPSICUM ANNUUM, FUCUS VESICULOSUS, GALIUM APARINE, GARCINIA CAMBOGIA, HAMAMELIS VIRGINIANA, HEPAR SUIS, HISTAMINUM HYDROCHLORICUM, NUX VOMICA, PANCREAS SUIS, PETROSELINUM SATIVUM, THUJA OCCIDENTALIS, THYROIDINUM SUIS, ZINGIBER OFFICINALE openfda.generic_name manufacturer name Liddell Laboratories, Inc. openfda.manufacturer_name ndc package 50845-0232-2 openfda.package_ndc ndc package 50845-0232-1 openfda.package_ndc ndc product 50845-0232 openfda.product_ndc ndc11 package 50845023202 derived:openfda.package_ndc ndc11 package 50845023201 derived:openfda.package_ndc spl id 7498b0f5-fe09-482d-8a6c-c59066623800 id spl set id fbdf83c5-bc84-485e-8744-01b0bc504138 set_id unii 6RV024OAUQ openfda.unii unii 00UK7646FG openfda.unii unii D0QJI8UQVR openfda.unii unii 269XH13919 openfda.unii unii 3POA0Q644U openfda.unii unii F79059A38U openfda.unii unii 1NT28V9397 openfda.unii unii 535G2ABX9M openfda.unii unii 1WZA4Y92EX openfda.unii unii 7S82P3R43Z openfda.unii unii Z4B6561488 openfda.unii unii C5529G5JPQ openfda.unii unii 6EC706HI7F openfda.unii unii T7S323PKJS openfda.unii unii 9Y3J3362RY 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, 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 doctor before using product. Other information Store at room temperature. Do not use if TAMPER EVIDENT seal around neck of bottle is missing or broken.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.