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: 2026-10-12
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/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:30:54

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		knDR SANITIZER	openfda.brand_name
generic name		ALCOHOL	openfda.generic_name
manufacturer name		CROP BEAUTY GROUP INC.	openfda.manufacturer_name
ndc	package	78768-004-30	openfda.package_ndc
ndc	product	78768-004	openfda.product_ndc
ndc11	package	78768000430	derived:openfda.package_ndc
rxcui		581660	openfda.rxcui
spl id		0897b5ff-cabe-5ed5-e063-6294a90a92ee	id
spl set id		97f125d7-9ee9-4a0e-99e8-798df7ebb0ff	set_id
unii		3K9958V90M	openfda.unii

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.

Reported adverse events (FAERS/openFDA)#

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