DermaCen Instant Hand Sanitizer with Aloe

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: DermaCen Instant Hand Sanitizer with Aloe
Generic name: ALCOHOL
Manufacturer: Central Solutions Inc
Product type: HUMAN OTC DRUG
SPL set ID: dc6191ae-841f-48b6-b454-72d8d43fdcce
SPL ID: 28d9bd0b-15c2-c409-e063-6294a90a4619
Version: 8
Effective date: 2024-12-09
Source export date: 2026-09-28
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/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:24:34

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 · 25 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		DermaCen Instant Hand Sanitizer with Aloe	openfda.brand_name
generic name		ALCOHOL	openfda.generic_name
manufacturer name		Central Solutions Inc	openfda.manufacturer_name
ndc	package	62654-143-19	openfda.package_ndc
ndc	package	62654-143-04	openfda.package_ndc
ndc	package	62654-143-37	openfda.package_ndc
ndc	package	62654-143-03	openfda.package_ndc
ndc	package	62654-143-92	openfda.package_ndc
ndc	package	62654-143-06	openfda.package_ndc
ndc	package	62654-143-02	openfda.package_ndc
ndc	package	62654-143-12	openfda.package_ndc
ndc	product	62654-143	openfda.product_ndc
ndc11	package	62654014392	derived:openfda.package_ndc
ndc11	package	62654014303	derived:openfda.package_ndc
ndc11	package	62654014304	derived:openfda.package_ndc
ndc11	package	62654014312	derived:openfda.package_ndc
ndc11	package	62654014302	derived:openfda.package_ndc
ndc11	package	62654014337	derived:openfda.package_ndc
ndc11	package	62654014306	derived:openfda.package_ndc
ndc11	package	62654014319	derived:openfda.package_ndc
rxcui		1145610	openfda.rxcui
spl id		28d9bd0b-15c2-c409-e063-6294a90a4619	id
spl set id		dc6191ae-841f-48b6-b454-72d8d43fdcce	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 Avoid contact with eyes In case of eye contact, flush with water for 15 minutes Discontinue use and see a doctor if irritation occurs Avoid contact with broken skin. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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