FDA.reportPublic FDA data

knDR 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
knDR SANITIZER
Generic name
ALCOHOL
Manufacturer
CROP BEAUTY GROUP INC.
Product type
HUMAN OTC DRUG
SPL set ID
97f125d7-9ee9-4a0e-99e8-798df7ebb0ff
SPL ID
0897b5ff-cabe-5ed5-e063-6294a90a92ee
Version
2
Effective date
2023-10-26
Source export date
2026-08-01
Source partition
3
Source file
https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-08-01/286b06ef66f7efdb8cdf48688678b429950d1b94558fe44fcd6cc6eb20c2100b/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:03:43
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 and flame When using this product Avoid the eyes and mucous membranes. In the case of eyes or mucous membranes contact,rinse area thoroughly with water. Stop use and ask a doctor if Condition worsens. Redness or irritation develops. Condition persists for more than 3 days. Keep out of reach of children. If swallowed,contact a doctor or Poison Control Center immediately.