FORPRO PROFESSIONAL COLLECTION ALCOHOL-FREE FOAMING INSTANT HAND SANITIZER- benzalkonium chloride liquid

ForPro Professional Collection Alcohol-Free Foaming Instant Hand Sanitizer by

Drug Labeling and Warnings

ForPro Professional Collection Alcohol-Free Foaming Instant Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by R & R Lotion, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

Benzalkonium Chloride 0.1%

Purpose

Antiseptic

Uses

• Hand sanitizer to help reduce bacteria on the skin that can potentially cause disease.
• Recommended for repeated use.

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.

Directions

• Pump sufficient amount of foam into palm of hand.
• Wet all surfaces of both hands thoroughly with product, including the area under the fingernails and rub until dry.

Inactive Ingredients

DI Water, Cetrimonium Chloride, Laurtrimonium Chloride, Dihydroxyethyl Cocamine Oxide, Glycereth-17 Cocoate, Citric Acid

PRINCIPAL DISPLAY PANEL - 591 mL Bottle Label

ForPro®
Professional Collection

ALCOHOL-FREE

Foaming
Instant
Hand
Sanitizer

Kills germs in
15
seconds

Kills 99.99% of
most common germs

Moisturizing Dye & Fragrance Free

20 FL OZ (591mL) ℮

INGREDIENTS AND APPEARANCE

FORPRO PROFESSIONAL COLLECTION ALCOHOL-FREE FOAMING INSTANT HAND SANITIZER 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59555-404
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Benzalkonium Chloride (UNII: F5UM2KM3W7) (Benzalkonium - UNII:7N6JUD5X6Y)	Benzalkonium Chloride	1 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Cetrimonium Chloride (UNII: UC9PE95IBP)
Laurtrimonium Chloride (UNII: A81MSI0FIC)
Dihydroxyethyl Cocamine Oxide (UNII: 8AR51R3BL5)
Glycereth-17 Cocoate (UNII: 3057VPT0KC)
Citric Acid Monohydrate (UNII: 2968PHW8QP)

Product Characteristics
Color	WHITE	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59555-404-12	591 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/28/2025
2	NDC: 59555-404-11	3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/28/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	05/28/2025

Labeler - R & R Lotion, Inc (062979000)