Home FDA labels b274cc51-dd50-430a-bc9e-ad8c1b6be455 ANXIETY II HP 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 ANXIETY II HP
Generic name ACONITUM NAPELLUS, ARSENIC TRIOXIDE, ATROPA BELLADONNA, OYSTER SHELL CALCIUM CARBONATE, CRUDE, ACTIVATED CHARCOAL, HUMAN BREAST TUMOR CELL, CAUSTICUM, GELSEMIUM SEMPERVIRENS ROOT, LACHESIS MUTA VENOM, MERCURY, SODIUM CHLORIDE, NITRIC ACID, PHOSPHORUS, TOXICODENDRON PUBESCENS LEAF
Manufacturer Natural Creations, Inc.
Product type HUMAN OTC DRUG
SPL set ID 02fa45a5-08e1-41ad-acd4-0f85db07e89e
SPL ID b274cc51-dd50-430a-bc9e-ad8c1b6be455
Version 4
Effective date 2025-11-13
Source export date 2026-10-12
Source partition 3
Source file https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 01:32:34 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 · 22 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name ANXIETY II HP openfda.brand_name generic name ACONITUM NAPELLUS, ARSENIC TRIOXIDE, ATROPA BELLADONNA, OYSTER SHELL CALCIUM CARBONATE, CRUDE, ACTIVATED CHARCOAL, HUMAN BREAST TUMOR CELL, CAUSTICUM, GELSEMIUM SEMPERVIRENS ROOT, LACHESIS MUTA VENOM, MERCURY, SODIUM CHLORIDE, NITRIC ACID, PHOSPHORUS, TOXICODENDRON PUBESCENS LEAF openfda.generic_name manufacturer name Natural Creations, Inc. openfda.manufacturer_name ndc package 43406-0004-1 openfda.package_ndc ndc product 43406-0004 openfda.product_ndc ndc11 package 43406000401 derived:openfda.package_ndc spl id b274cc51-dd50-430a-bc9e-ad8c1b6be455 id spl set id 02fa45a5-08e1-41ad-acd4-0f85db07e89e set_id unii 2P3VWU3H10 openfda.unii unii 27YLU75U4W openfda.unii unii DD5FO1WKFU openfda.unii unii 411VRN1TV4 openfda.unii unii FXS1BY2PGL openfda.unii unii 639KR60Q1Q openfda.unii unii 451W47IQ8X openfda.unii unii 2E32821G6I openfda.unii unii 6IO182RP7A openfda.unii unii S7V92P67HO openfda.unii unii C62OO7VD9K openfda.unii unii WQZ3G9PF0H openfda.unii unii VSW71SS07I openfda.unii unii U0NQ8555JD 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: Consult a physician for use in chlidren under 12 years of age. IF PRAGNANT OR BREAST-FEEDING, ask a health care professional before use. KEEP OUT OF THE REACH OF CHILDREN. In case of overdose (or accidential ingestion) get medical help or contact a Poison Control Center right away. Do not use if TAMPER EVIDENT seal is broken or missing.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.