TECHNI-PRO FOAMING HAND SANITIZER- benzalkonium chloride liquid

Techni-Pro Foaming Hand Sanitizer by

Drug Labeling and Warnings

Techni-Pro Foaming 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

Antimicrobial

Uses

• For hand sanitizing to decrease bacteria on the skin
• Recommended for repeated use

Warnings

For external use only

When using this product avoid contact with eyes. If contact with eyes, flush with water.

Stop use and ask a doctor if irritation or redness develops, or if condition persists for 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 a small amount of foam into palm of hand
• Rub thoroughly over all surfaces of both hands
• Rub hands together briskly until dry.

Inactive Ingredients

DI Water, Dihydroxypropyl PEG-5 Linoleammonium Chloride, Glycereth-2 Ocoate, Behentrimonium Chloride, Dihydroxyethyl Cocamine Oxide

PRINCIPAL DISPLAY PANEL - 3785 mL Bottle Label

TECHNI-PRO

FOAMING
HAND SANITIZER

TestEquity Part #:
TNP-ICHS-GAL

PACKAGING SIZE: 128oz.

INGREDIENTS AND APPEARANCE

TECHNI-PRO FOAMING HAND SANITIZER 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59555-403
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: 59555-403-12	591 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	03/10/2022
2	NDC: 59555-403-11	3785 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	03/10/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part333A	03/10/2022

Labeler - R & R Lotion, Inc (062979000)