WhiskCare 367

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: WhiskCare 367
Generic name: CHLOROXYLENOL
Manufacturer: Whisk Products, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: ec8f74f1-fe58-4e89-bbb1-59f057278293
SPL ID: 11fe5b32-9dfb-adb9-e063-6294a90a5b68
Version: 7
Effective date: 2024-02-22
Source export date: 2026-09-28
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:24:02

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 · 25 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		WhiskCare 367	openfda.brand_name
generic name		CHLOROXYLENOL	openfda.generic_name
manufacturer name		Whisk Products, Inc.	openfda.manufacturer_name
ndc	package	65585-568-08	openfda.package_ndc
ndc	package	65585-568-03	openfda.package_ndc
ndc	package	65585-568-05	openfda.package_ndc
ndc	package	65585-568-02	openfda.package_ndc
ndc	package	65585-568-07	openfda.package_ndc
ndc	package	65585-568-04	openfda.package_ndc
ndc	package	65585-568-01	openfda.package_ndc
ndc	package	65585-568-06	openfda.package_ndc
ndc	product	65585-568	openfda.product_ndc
ndc11	package	65585056803	derived:openfda.package_ndc
ndc11	package	65585056805	derived:openfda.package_ndc
ndc11	package	65585056807	derived:openfda.package_ndc
ndc11	package	65585056808	derived:openfda.package_ndc
ndc11	package	65585056801	derived:openfda.package_ndc
ndc11	package	65585056806	derived:openfda.package_ndc
ndc11	package	65585056802	derived:openfda.package_ndc
ndc11	package	65585056804	derived:openfda.package_ndc
rxcui		1045003	openfda.rxcui
spl id		11fe5b32-9dfb-adb9-e063-6294a90a5b68	id
spl set id		ec8f74f1-fe58-4e89-bbb1-59f057278293	set_id
unii		0F32U78V2Q	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. Do not use in eyes. Discontinue use if irritation and redness develop. If condition persists for more than 72 hours, consult a physician. Not for use on children under six months of age. For institutional and professional use only.

Reported adverse events (FAERS/openFDA)#

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