AZX Wellness Hand Sanitizer

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
AZX Wellness Hand Sanitizer
Generic name
ALCOHOL
Manufacturer
ASC Marketing LTD
Product type
HUMAN OTC DRUG
SPL set ID
b57c7e3a-f0bf-fd42-e053-2a95a90a3b4f
SPL ID
0b6dc42e-c0ac-b6cf-e063-6294a90aef5b
Version
2
Effective date
2023-12-01
Source export date
2026-10-27
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-27/35717de05250cd386420cc8ede3b6010b48d18eea2af59afb0617fcabca634ec/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run
20261027T193451Z
Imported at
2026-10-27 20:04:15
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. Flammable. Keep away from fire or flames. Do not use in the eyes. In case of contact, rinse eyes thoroughly with water. Stop use and ask a doctor if irritation or redness develop and persist for more than 72 hours. Keep out of reach of children. If swallowed get medical help or contact Poison Control Center right away. Store between 59-86°F (15-30°C). Avoid freezing and excessive heat above 104°F (40°C).

Reported adverse events (FAERS/openFDA)#

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