DETRAPEL HAND SANITIZER- benzalkonium chloride soap

DetraPel Hand Sanitizer by

Drug Labeling and Warnings

DetraPel Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by DetraPel, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

• Active Ingredient: Purpose
• Benzalkonium Chloride 0.13% .............: 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. In case of eye contact, flush eyes with water.

Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours.

Directions

• Spray a small amount of liquid into palm of hand
• Rub thorougly over all surfaces of both hands
• Rub hands together briskly until dry

Inactive Ingredients

Water, dihyroxypropyl PEG-5 linoleammonium chloride, glycereth-2 cocoate, behentrimonium chloride, dihydroxyethyl cocamine oxide, fragrance.

Uses

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

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

PRINCIPAL DISPLAY PANEL

DetraPel Hand Sanitizer

INGREDIENTS AND APPEARANCE

DETRAPEL HAND SANITIZER 
benzalkonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74961-2300(NDC:71023-445)
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
DIHYDROXYETHYL COCAMINE OXIDE (UNII: 8AR51R3BL5)
DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE (UNII: 0Y0NQR2GH1)
WATER (UNII: 059QF0KO0R)
GLYCERETH-2 COCOATE (UNII: JWM00VS7HC)
BEHENTRIMONIUM CHLORIDE (UNII: X7GNG3S47T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74961-2300-2	200 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	04/23/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/23/2020

Labeler - DetraPel, Inc. (081308287)

Establishment
Name	Address	ID/FEI	Business Operations
DetraPel, Inc.		081308287	relabel(74961-2300) , repack(74961-2300)