ForPro Professional Collection Alcohol-Free Foaming Instant Hand Sanitizer - Cucumber Mint Bliss

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 - Cucumber Mint Bliss
Generic name: BENZALKONIUM CHLORIDE
Manufacturer: R & R Lotion, Inc
Product type: HUMAN OTC DRUG
SPL set ID: 458dec24-b5bb-240a-e063-6294a90a81f3
SPL ID: 458dec24-b5bc-240a-e063-6294a90a81f3
Version: 1
Effective date: 2026-02-11
Source export date: 2026-10-12
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/b939c18fdf51df171cf60ce5558819d08ac66bb16bb9991d48cbec91028d783e/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:38:51

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 - Cucumber Mint Bliss	openfda.brand_name
generic name		BENZALKONIUM CHLORIDE	openfda.generic_name
manufacturer name		R & R Lotion, Inc	openfda.manufacturer_name
ndc	package	59555-405-12	openfda.package_ndc
ndc	package	59555-405-11	openfda.package_ndc
ndc	package	59555-405-13	openfda.package_ndc
ndc	product	59555-405	openfda.product_ndc
ndc11	package	59555040511	derived:openfda.package_ndc
ndc11	package	59555040513	derived:openfda.package_ndc
ndc11	package	59555040512	derived:openfda.package_ndc
rxcui		1038799	openfda.rxcui
spl id		458dec24-b5bc-240a-e063-6294a90a81f3	id
spl set id		458dec24-b5bb-240a-e063-6294a90a81f3	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.