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
bf0098ab-6c0d-ecd2-e053-2a95a90a670c
SPL ID
0b6e0202-cdf3-d783-e063-6394a90a3bf2
Version
2
Effective date
2023-12-01
Source export date
2026-09-28
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:44:18
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 Do not use in eyes. Discontinue use if irritation and redness develop. Flammable, keep away from fire or flame. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Centre right away. If pregnant or breast-feeding, ask a health professional before use.

Reported adverse events (FAERS/openFDA)#

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