WhiskCare 362

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 362
Generic name: CHLOROXYLENOL
Manufacturer: Whisk Products, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: c69abe4e-03bf-456e-8be3-35d3c8720228
SPL ID: 0b750715-f199-3f7b-e063-6394a90a876e
Version: 4
Effective date: 2023-12-01
Source export date: 2026-10-12
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/2026-10-12/b939c18fdf51df171cf60ce5558819d08ac66bb16bb9991d48cbec91028d783e/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:36:59

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 362	openfda.brand_name
generic name		CHLOROXYLENOL	openfda.generic_name
manufacturer name		Whisk Products, Inc.	openfda.manufacturer_name
ndc	package	65585-562-01	openfda.package_ndc
ndc	package	65585-562-07	openfda.package_ndc
ndc	package	65585-562-05	openfda.package_ndc
ndc	package	65585-562-02	openfda.package_ndc
ndc	package	65585-562-06	openfda.package_ndc
ndc	package	65585-562-04	openfda.package_ndc
ndc	package	65585-562-10	openfda.package_ndc
ndc	package	65585-562-13	openfda.package_ndc
ndc	package	65585-562-09	openfda.package_ndc
ndc	package	65585-562-08	openfda.package_ndc
ndc	package	65585-562-12	openfda.package_ndc
ndc	package	65585-562-03	openfda.package_ndc
ndc	package	65585-562-11	openfda.package_ndc
ndc	product	65585-562	openfda.product_ndc
ndc11	package	65585056208	derived:openfda.package_ndc
ndc11	package	65585056212	derived:openfda.package_ndc
ndc11	package	65585056210	derived:openfda.package_ndc
ndc11	package	65585056213	derived:openfda.package_ndc
ndc11	package	65585056201	derived:openfda.package_ndc
ndc11	package	65585056204	derived:openfda.package_ndc
ndc11	package	65585056211	derived:openfda.package_ndc
ndc11	package	65585056202	derived:openfda.package_ndc
ndc11	package	65585056207	derived:openfda.package_ndc
ndc11	package	65585056206	derived:openfda.package_ndc
ndc11	package	65585056205	derived:openfda.package_ndc
ndc11	package	65585056203	derived:openfda.package_ndc
ndc11	package	65585056209	derived:openfda.package_ndc
rxcui		1045003	openfda.rxcui
spl id		0b750715-f199-3f7b-e063-6394a90a876e	id
spl set id		c69abe4e-03bf-456e-8be3-35d3c8720228	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 6 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.