Home FDA labels 456fc8b1-a255-4144-961d-73a922afadda VertiFix 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 VertiFix
Generic name ARGENTUM NITRICUM, BRYONIA (ALBA), CAUSTICUM, COCCULUS INDICUS, GELSEMIUM SEMPERVIRENS, IPECACUANHA, NUX VOMICA, PETROLEUM, SULPHUR, TABACUM
Manufacturer NaturalCare
Product type HUMAN OTC DRUG
SPL set ID 33b00f06-3202-4904-855c-cdfaa93677a4
SPL ID 456fc8b1-a255-4144-961d-73a922afadda
Version 2
Effective date 2026-08-27
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 01:32:54 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 · 18 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name VertiFix openfda.brand_name generic name ARGENTUM NITRICUM, BRYONIA (ALBA), CAUSTICUM, COCCULUS INDICUS, GELSEMIUM SEMPERVIRENS, IPECACUANHA, NUX VOMICA, PETROLEUM, SULPHUR, TABACUM openfda.generic_name manufacturer name NaturalCare openfda.manufacturer_name ndc package 70163-0008-1 openfda.package_ndc ndc product 70163-0008 openfda.product_ndc ndc11 package 70163000801 derived:openfda.package_ndc spl id 456fc8b1-a255-4144-961d-73a922afadda id spl set id 33b00f06-3202-4904-855c-cdfaa93677a4 set_id unii 269XH13919 openfda.unii unii DD5FO1WKFU openfda.unii unii 639KR60Q1Q openfda.unii unii 6YR2608RSU openfda.unii unii 95IT3W8JZE openfda.unii unii 62I3C8233L openfda.unii unii T7J046YI2B openfda.unii unii 70FD1KFU70 openfda.unii unii 810258W28U openfda.unii unii 1C89KKC04E 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: Stop use and ask a doctor if ■ symptoms worsen or persist for more than 7 days ■ new symptoms appear ■ symptoms are severe If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children . In case of overdose, get medical help or contact a Poison Control Center right away. Do not use if printed foil blister is broken or missing. ■ Store at room temperature (65-80ºF)
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.