Avant Alcohol-Free Instant Hand Sanitizer

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: Avant Alcohol-Free Instant Hand Sanitizer
Generic name: BENZALKONIUM CHLORIDE
Manufacturer: B4 Soap LLC
Product type: HUMAN OTC DRUG
SPL set ID: ec561e3b-996e-484a-af64-f388f0fbfe5b
SPL ID: 4d3d6788-4fe7-beb5-e063-6294a90a16ec
Version: 10
Effective date: 2026-03-17
Source export date: 2026-09-28
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:27:11

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 · 20 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		Avant Alcohol-Free Instant Hand Sanitizer	openfda.brand_name
generic name		BENZALKONIUM CHLORIDE	openfda.generic_name
manufacturer name		B4 Soap LLC	openfda.manufacturer_name
ndc	package	68306-112-03	openfda.package_ndc
ndc	package	68306-112-06	openfda.package_ndc
ndc	package	68306-112-01	openfda.package_ndc
ndc	package	68306-112-05	openfda.package_ndc
ndc	package	68306-112-02	openfda.package_ndc
ndc	package	68306-112-04	openfda.package_ndc
ndc	product	68306-112	openfda.product_ndc
ndc11	package	68306011204	derived:openfda.package_ndc
ndc11	package	68306011205	derived:openfda.package_ndc
ndc11	package	68306011203	derived:openfda.package_ndc
ndc11	package	68306011202	derived:openfda.package_ndc
ndc11	package	68306011201	derived:openfda.package_ndc
ndc11	package	68306011206	derived:openfda.package_ndc
spl id		4d3d6788-4fe7-beb5-e063-6294a90a16ec	id
spl set id		ec561e3b-996e-484a-af64-f388f0fbfe5b	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 . Do not use in the eyes. In case of eye contact, flush thoroughly with water and seek medical attention. Stop use and ask doctor if irritation and redness develop and persists for more than 72 hours. 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.