KeriCure 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
KeriCure Hand Sanitizer
Generic name
ALCOHOL
Manufacturer
Kericure Inc.
Product type
HUMAN OTC DRUG
SPL set ID
40d283ad-38a8-4ee6-bcba-56ccb99f7ee6
SPL ID
3a859c6d-fd08-4d43-b77f-23ffcc00f5d3
Version
2
Effective date
2025-01-22
Source export date
2026-10-12
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/2026-10-12/13cbfcd236c665f0ee69e2d9141331148dcdff45d1679c92f029cfba27dd74a2/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:44:28
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 heat or flame • Do not use on children less than 2 month of age on open skin wounds • When using this product keep out of eyes, ears and mouth • In case of contact with eyes, rinse eyes thoroughly with water • Do NOT ingest • Keep out of reach of children • If swallowed, seek 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.