Sugarcoat Hand Sanitizer

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: Sugarcoat Hand Sanitizer
Generic name: ETHYL ALCOHOL
Manufacturer: PEACH LAYNE, LLC
Product type: HUMAN OTC DRUG
SPL set ID: 5570284d-0872-1fee-e063-6294a90a9b65
SPL ID: 557017d4-2862-39bd-e063-6394a90a6e4b
Version: 1
Effective date: 2026-07-06
Source export date: 2026-11-06
Source partition: 7
Source file: https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/824fe785252d7061429a95ddb6de517ee399ef628d34e8fdcc3591ded286ae33/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 07:27:09

Harmonized routes table
Harmonized routes
TOPICAL

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		Sugarcoat Hand Sanitizer	openfda.brand_name
generic name		ETHYL ALCOHOL	openfda.generic_name
manufacturer name		PEACH LAYNE, LLC	openfda.manufacturer_name
ndc	package	87361-006-01	openfda.package_ndc
ndc	product	87361-006	openfda.product_ndc
ndc11	package	87361000601	derived:openfda.package_ndc
rxcui		1041849	openfda.rxcui
spl id		557017d4-2862-39bd-e063-6394a90a6e4b	id
spl set id		5570284d-0872-1fee-e063-6294a90a9b65	set_id
unii		3K9958V90M	openfda.unii

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

Warnings For external use only. Flammable, keep away form fire or flame. May Cause Serious Irritation In Case of Direct Eye Contact.

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