Home FDA labels 6b95574e-24cf-4cb9-a23a-284c2981fa33 Frenna AC 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 Frenna AC
Generic name ALUMINUM CHLORIDE
Manufacturer Dharma Research, inc.
Product type HUMAN PRESCRIPTION DRUG
SPL set ID d09ae142-6fd5-45e4-a9c4-44428885ccaf
SPL ID 6b95574e-24cf-4cb9-a23a-284c2981fa33
Version 2
Effective date 2020-11-06
Source export date 2026-10-12
Source partition 8
Source file https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 02:09:24 Harmonized routes table Harmonized routes DENTAL, ORAL, TOPICAL
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 · 10 matching rows.
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 and cautions Discontinue use if irritation appears. For topical application only. Avoid eye contact. Do not use in patients with a known history of hyper sensetivity to Aluminum Chloride. For professional use only. Federal law restricts this product to sale or use on the order of a dentist.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.