FDA.reportPublic FDA data

ForPro Professional Collection Alcohol-Free Foaming Instant Hand Sanitizer

Manufacturer
Sani-care Salon Products, Inc.
Effective date
2024-07-09
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 00:15:03

Label at a glance#

ProductForPro Professional Collection Alcohol-Free Foaming Instant Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of ChildrenKeep out of reach of Children

OTC - PURPOSE SECTION

Purpose sectionPurpose section

OTC - ACTIVE INGREDIENT SECTION

OTC active ingredienntOTC active ingrediennt

DOSAGE & ADMINISTRATION SECTION

DosageDosage

INACTIVE INGREDIENT SECTION

inactive ingredientsinactive ingredients

INDICATIONS & USAGE SECTION

UsageUsage

WARNINGS SECTION

Warnings SectionWarnings Section

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Packaging labelPackaging label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038799benzalkonium chloride 0.1 % Topical FoamPSN5
1038799benzalkonium chloride 1 MG/ML Topical FoamSCD5
1038799benzalkonium chloride 0.1 % Topical FoamSY5

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72671-100-02ForPro Professional Collection Alcohol-Free Foaming Instant Hand Sanitizer00 mL in 1 BOTTLELIQUID005

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72671-100FORPRO PROFESSIONAL COLLECTION ALCOHOL-FREE FOAMING INSTANT HAND SANITIZER (BENZALKONIUM CHLORIDE) LIQUID [SANI-CARE SALON PRODUCTS, INC.]5Legacy NDC, 1 package rows20240711_b6ab77bb-7cbb-80ee-e053-2a95a90a48c3.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72671-10072671-100-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
1cd39837-e040-a58d-e063-6294a90a9cd5b6ab77bb-7cbb-80ee-e053-2a95a90a48c32024-07-09WarningsExact identifier
spl id: 1cd39837-e040-a58d-e063-6294a90a9cd5
spl set id: b6ab77bb-7cbb-80ee-e053-2a95a90a48c3

Reported adverse events (FAERS/openFDA)#

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