WhiskCare 365

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 365
Generic name: CHLOROXYLENOL
Manufacturer: Whisk Products, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 420f941d-8ed0-42f4-901a-b04b29b51da6
SPL ID: 0b756336-e229-c53b-e063-6294a90a6fec
Version: 5
Effective date: 2023-12-01
Source export date: 2026-09-28
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/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:17:50

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 · 35 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		WhiskCare 365	openfda.brand_name
generic name		CHLOROXYLENOL	openfda.generic_name
manufacturer name		Whisk Products, Inc.	openfda.manufacturer_name
ndc	package	65585-365-09	openfda.package_ndc
ndc	package	65585-365-12	openfda.package_ndc
ndc	package	65585-365-11	openfda.package_ndc
ndc	package	65585-365-01	openfda.package_ndc
ndc	package	65585-365-04	openfda.package_ndc
ndc	package	65585-365-02	openfda.package_ndc
ndc	package	65585-365-10	openfda.package_ndc
ndc	package	65585-365-08	openfda.package_ndc
ndc	package	65585-365-03	openfda.package_ndc
ndc	package	65585-365-13	openfda.package_ndc
ndc	package	65585-365-07	openfda.package_ndc
ndc	package	65585-365-05	openfda.package_ndc
ndc	package	65585-365-06	openfda.package_ndc
ndc	product	65585-365	openfda.product_ndc
ndc11	package	65585036511	derived:openfda.package_ndc
ndc11	package	65585036509	derived:openfda.package_ndc
ndc11	package	65585036508	derived:openfda.package_ndc
ndc11	package	65585036505	derived:openfda.package_ndc
ndc11	package	65585036506	derived:openfda.package_ndc
ndc11	package	65585036504	derived:openfda.package_ndc
ndc11	package	65585036513	derived:openfda.package_ndc
ndc11	package	65585036502	derived:openfda.package_ndc
ndc11	package	65585036501	derived:openfda.package_ndc
ndc11	package	65585036503	derived:openfda.package_ndc
ndc11	package	65585036510	derived:openfda.package_ndc
ndc11	package	65585036507	derived:openfda.package_ndc
ndc11	package	65585036512	derived:openfda.package_ndc
rxcui		413257	openfda.rxcui
spl id		0b756336-e229-c53b-e063-6294a90a6fec	id
spl set id		420f941d-8ed0-42f4-901a-b04b29b51da6	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.