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

ForPro Professional Collection Alcohol-Free Foaming Instant Hand Sanitizer - Vanilla Sugar Bliss by

Drug Labeling and Warnings

ForPro Professional Collection Alcohol-Free Foaming Instant Hand Sanitizer - Vanilla Sugar Bliss 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:

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

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-free
VANILLA SUGAR BLISS

20 FL OZ (591mL) ℮

INGREDIENTS AND APPEARANCE

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

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59555-406
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
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
WATER (UNII: 059QF0KO0R)
DIHYDROXYETHYL COCAMINE OXIDE (UNII: 8AR51R3BL5)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC)
GLYCERETH-17 COCOATE (UNII: 3057VPT0KC)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59555-406-11	3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/20/2026
2	NDC: 59555-406-12	591 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	01/20/2026
3	NDC: 59555-406-13	50 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	01/20/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	01/20/2026

Labeler - R & R Lotion, Inc (062979000)