Sani Professional Brand Sani-Hands for Kids Instant Hand Sanitizing Wipes

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: Sani Professional Brand Sani-Hands for Kids Instant Hand Sanitizing Wipes
Generic name: ALCOHOL
Manufacturer: Professional Disposables International, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 8a1a3adf-9b9c-4251-ba88-d7314c855b2b
SPL ID: 43408dfd-0e86-a56d-e063-6294a90aa418
Version: 2
Effective date: 2025-11-10
Source export date: 2026-09-28
Source partition: 6
Source file: https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:34:32

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 · 15 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		Sani Professional Brand Sani-Hands for Kids Instant Hand Sanitizing Wipes	openfda.brand_name
generic name		ALCOHOL	openfda.generic_name
manufacturer name		Professional Disposables International, Inc.	openfda.manufacturer_name
ndc	package	10819-7004-4	openfda.package_ndc
ndc	package	10819-7004-3	openfda.package_ndc
ndc	package	10819-7004-5	openfda.package_ndc
ndc	product	10819-7004	openfda.product_ndc
ndc11	package	10819700405	derived:openfda.package_ndc
ndc11	package	10819700403	derived:openfda.package_ndc
ndc11	package	10819700404	derived:openfda.package_ndc
rxcui		1251416	openfda.rxcui
spl id		43408dfd-0e86-a56d-e063-6294a90aa418	id
spl set id		8a1a3adf-9b9c-4251-ba88-d7314c855b2b	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

Flammable, keep away from fire or flame. For external use only. Do not use in or contact the eyes. Discontinue use if irritation and redness develop. If condition persist for more than 72 hours consult a physician. If swallowed, get medical help or contact a Poison Control Center immediately. Keep this out of reach of children unless under adult supervision.

Reported adverse events (FAERS/openFDA)#

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