ZO Skin Health Astringent Solution

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
ZO Skin Health Astringent Solution
Generic name
ALUMINUM ACETATE
Manufacturer
ZO Skin Health, Inc.
Product type
HUMAN OTC DRUG
SPL set ID
cb801d7e-52ad-6c16-e053-2a95a90a7a1f
SPL ID
25ca3908-24a9-5e4f-e063-6394a90a7a88
Version
6
Effective date
2024-10-31
Source export date
2026-11-06
Source partition
9
Source file
https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/423686b2ac39507df6931677ae004637f2f017f82cbe44b047a75ba358b9d453/drug-label-0009-of-0014.json.zip
Source manifest SHA-256
8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
Import run
20261106T075659Z
Imported at
2026-11-06 08:57:35
Harmonized routes table
Harmonized routes
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

Warnings For external use only. When using this product ■ avoid contact with eyes. If contact occurs, rinse thoroughly with water. ■ do not cover compress or wet dressing with plastic to prevent evaporation ■ in some skin conditions, soaking too long may overdry Stop use and ask a doctor ■ if condition worsens or symptoms persist for more than 7 days Keep out of reach of children. ■ if swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.