MaxSaver 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: MaxSaver Sanitizing Wipes
Generic name: BENZALKONIUM CHLORIDE
Manufacturer: Innocore Sales & Marketing Inc
Product type: HUMAN OTC DRUG
SPL set ID: 00ccdb15-7db9-0102-e063-6294a90a3ee3
SPL ID: 56d4a790-f150-1f42-e063-6394a90ae0ba
Version: 6
Effective date: 2026-07-17
Source export date: 2026-11-06
Source partition: 6
Source file: https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/10387d7618367cd955339e75d48af3d11f99f789153db05c529d9fad6eccc645/drug-label-0006-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 07:18:34

Harmonized routes table
Harmonized routes
CUTANEOUS

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		MaxSaver Sanitizing Wipes	openfda.brand_name
generic name		BENZALKONIUM CHLORIDE	openfda.generic_name
manufacturer name		Innocore Sales & Marketing Inc	openfda.manufacturer_name
ndc	package	70924-005-03	openfda.package_ndc
ndc	package	70924-005-02	openfda.package_ndc
ndc	package	70924-005-04	openfda.package_ndc
ndc	package	70924-005-01	openfda.package_ndc
ndc	product	70924-005	openfda.product_ndc
ndc11	package	70924000503	derived:openfda.package_ndc
ndc11	package	70924000504	derived:openfda.package_ndc
ndc11	package	70924000501	derived:openfda.package_ndc
ndc11	package	70924000502	derived:openfda.package_ndc
rxcui		1038558	openfda.rxcui
spl id		56d4a790-f150-1f42-e063-6394a90ae0ba	id
spl set id		00ccdb15-7db9-0102-e063-6294a90a3ee3	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 For external use only. When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly in water. Discontinue use if irritation and redness develop. If conditions persist for more than 72 hours, consult a physician. If swallowed get medical help or contact a poison control center immediately. Keep out of reach of children.

Reported adverse events (FAERS/openFDA)#

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