MagiCare Premium 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: MagiCare Premium Hand Sanitizing Wipes
Generic name: ALCOHOL
Manufacturer: MAGICARE TECH CORP
Product type: HUMAN OTC DRUG
SPL set ID: 3113dd38-257e-4b30-a611-1f259d1e3d1b
SPL ID: 58bb9de2-54a7-cafd-e063-6294a90a4cfc
Version: 3
Effective date: 2026-08-10
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 06:18:44

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 · 17 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		MagiCare Premium Hand Sanitizing Wipes	openfda.brand_name
generic name		ALCOHOL	openfda.generic_name
manufacturer name		MAGICARE TECH CORP	openfda.manufacturer_name
ndc	package	85276-104-02	openfda.package_ndc
ndc	package	85276-104-01	openfda.package_ndc
ndc	package	85276-104-04	openfda.package_ndc
ndc	package	85276-104-03	openfda.package_ndc
ndc	product	85276-104	openfda.product_ndc
ndc11	package	85276010404	derived:openfda.package_ndc
ndc11	package	85276010401	derived:openfda.package_ndc
ndc11	package	85276010402	derived:openfda.package_ndc
ndc11	package	85276010403	derived:openfda.package_ndc
rxcui		1307051	openfda.rxcui
spl id		58bb9de2-54a7-cafd-e063-6294a90a4cfc	id
spl set id		3113dd38-257e-4b30-a611-1f259d1e3d1b	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: FLAMMABLE. KEEP AWAY FROM FIRE OR FLAME. • FOR EXTERNAL USE ONLY. DO NOT USE IN OR NEAR THE EYES. IN CASE OF CONTACT, RINSE EYES THOROUGHLY WITH WATER. STOP USE AND CONSULT WITH A PHYSICIAN IF IRRITATION DEVELOPS AND LASTS FOR MORE THAN 72 HOURS. KEEP OUT OF REACH OF CHILDREN. IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER IMMEDIATELY.

Reported adverse events (FAERS/openFDA)#

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