ALTA ANTIBACTERIAL 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: ALTA ANTIBACTERIAL HAND WIPES
Generic name: BENZALKONIUM CHLORIDE
Manufacturer: Alta Sales Inc
Product type: HUMAN OTC DRUG
SPL set ID: 9064a1b1-dd4a-4f74-99c4-5ea93b4be210
SPL ID: c7113faf-8233-4c31-ba0d-03c4266099f4
Version: 5
Effective date: 2026-07-20
Source export date: 2026-11-06
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/97001096994db9ca8cee114e6c3bb5298d3c573158ffc1ab8692d82e76a3eb40/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 06:56:05

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 · 15 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		ALTA ANTIBACTERIAL HAND WIPES	openfda.brand_name
generic name		BENZALKONIUM CHLORIDE	openfda.generic_name
manufacturer name		Alta Sales Inc	openfda.manufacturer_name
ndc	package	79165-777-80	openfda.package_ndc
ndc	package	79165-777-20	openfda.package_ndc
ndc	package	79165-777-90	openfda.package_ndc
ndc	product	79165-777	openfda.product_ndc
ndc11	package	79165077720	derived:openfda.package_ndc
ndc11	package	79165077790	derived:openfda.package_ndc
ndc11	package	79165077780	derived:openfda.package_ndc
rxcui		1038558	openfda.rxcui
spl id		c7113faf-8233-4c31-ba0d-03c4266099f4	id
spl set id		9064a1b1-dd4a-4f74-99c4-5ea93b4be210	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 Keep out of eyes. In case of eye contact, rinse with water. If irritation develops, discontinue use. Consult a doctor if irritation persists more than 72 hours. If swallowed, seek medical attention or contact a Poison Control Center. Keep out of the children, except with adult supervision.

Reported adverse events (FAERS/openFDA)#

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