Hand Sanitizing Wipe

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: Hand Sanitizing Wipe
Generic name: ALCOHOL
Manufacturer: NeatGoods LLC
Product type: HUMAN OTC DRUG
SPL set ID: b700ff10-2836-7893-e053-2995a90a4322
SPL ID: 44e8813c-e338-9280-e063-6294a90a0b3a
Version: 4
Effective date: 2025-12-01
Source export date: 2026-09-28
Source partition: 11
Source file: https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:16:54

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		Hand Sanitizing Wipe	openfda.brand_name
generic name		ALCOHOL	openfda.generic_name
manufacturer name		NeatGoods LLC	openfda.manufacturer_name
ndc	package	81339-100-24	openfda.package_ndc
ndc	product	81339-100	openfda.product_ndc
ndc11	package	81339010024	derived:openfda.package_ndc
rxcui		884787	openfda.rxcui
spl id		44e8813c-e338-9280-e063-6294a90a0b3a	id
spl set id		b700ff10-2836-7893-e053-2995a90a4322	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 or flame. When using this product, do not use in or near eyes. If contact occurs, flush thoroughly with water. Stop use and contact a doctor if irritation or redness persists for more than 72 hours.

Reported adverse events (FAERS/openFDA)#

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