ForPro Professional Collection Alcohol-Free Foaming 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: ForPro Professional Collection Alcohol-Free Foaming Instant Hand Sanitizer
Generic name: BENZALKONIUM CHLORIDE
Manufacturer: R & R Lotion, Inc
Product type: HUMAN OTC DRUG
SPL set ID: 3ba7408c-7165-448c-b31c-9890807c0cb9
SPL ID: 4a7f8bd7-eb13-4f34-e063-6294a90a9eee
Version: 2
Effective date: 2026-02-11
Source export date: 2026-11-06
Source partition: 7
Source file: https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/824fe785252d7061429a95ddb6de517ee399ef628d34e8fdcc3591ded286ae33/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 07:27:19

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		ForPro Professional Collection Alcohol-Free Foaming Instant Hand Sanitizer	openfda.brand_name
generic name		BENZALKONIUM CHLORIDE	openfda.generic_name
manufacturer name		R & R Lotion, Inc	openfda.manufacturer_name
ndc	package	59555-404-13	openfda.package_ndc
ndc	package	59555-404-12	openfda.package_ndc
ndc	package	59555-404-11	openfda.package_ndc
ndc	product	59555-404	openfda.product_ndc
ndc11	package	59555040413	derived:openfda.package_ndc
ndc11	package	59555040412	derived:openfda.package_ndc
ndc11	package	59555040411	derived:openfda.package_ndc
rxcui		1038799	openfda.rxcui
spl id		4a7f8bd7-eb13-4f34-e063-6294a90a9eee	id
spl set id		3ba7408c-7165-448c-b31c-9890807c0cb9	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, ears or mouth. In case of eye contact, flush eyes with water. Stop use and ask a doctor if irritation and redness develop or if condition persists 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.