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

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.