My-Shield Sanitizing Hand 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: My-Shield Sanitizing Hand Wipes
Generic name: BENZALKONIUM CHLORIDE
Manufacturer: ENVIRO SPECIALTY CHEMICALS INC
Product type: HUMAN OTC DRUG
SPL set ID: ea99c72e-1881-498a-a653-29bac1dab97b
SPL ID: 464b00ba-8804-46db-8b45-e5b6f1829693
Version: 5
Effective date: 2026-07-21
Source export date: 2026-09-28
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:56:07

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 · 21 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		My-Shield Sanitizing Hand Wipes	openfda.brand_name
generic name		BENZALKONIUM CHLORIDE	openfda.generic_name
manufacturer name		ENVIRO SPECIALTY CHEMICALS INC	openfda.manufacturer_name
ndc	package	71884-010-80	openfda.package_ndc
ndc	package	71884-010-68	openfda.package_ndc
ndc	package	71884-010-20	openfda.package_ndc
ndc	package	71884-010-76	openfda.package_ndc
ndc	package	71884-010-82	openfda.package_ndc
ndc	package	71884-010-50	openfda.package_ndc
ndc	product	71884-010	openfda.product_ndc
ndc11	package	71884001082	derived:openfda.package_ndc
ndc11	package	71884001020	derived:openfda.package_ndc
ndc11	package	71884001076	derived:openfda.package_ndc
ndc11	package	71884001068	derived:openfda.package_ndc
ndc11	package	71884001050	derived:openfda.package_ndc
ndc11	package	71884001080	derived:openfda.package_ndc
rxcui		1038558	openfda.rxcui
spl id		464b00ba-8804-46db-8b45-e5b6f1829693	id
spl set id		ea99c72e-1881-498a-a653-29bac1dab97b	set_id
unii		F5UM2KM3W7	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: Do not freeze. For external use only. Do not use in ears, eyes or mouth. • When using this product, avoid contact with the eyes. In case of contact, flush eyes with water. • Stop use and ask a doctor if redness or irritation develop and persist for more than 72 hours. • Keep out of reach of children. • Children should be supervised when using this product.

Reported adverse events (FAERS/openFDA)#

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