Drug Details [pdf]

ANTISEPTIC WIPE- benzalkonium chloride patch
Total Resources International

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Active ingredient

Purpose - Benzalkonium Chloride 0.13% v/v....................Antiseptic

Uses

Antiseptic cleansing of face, hands and body to decrease bacteria on skin without soap and water

Warnings

For external use only.

Do not use in the eyes. If this happens, rinse thoroughly with water.

Stop use and ask a doctor if irritation or redness develop and 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

Tear open packet, unfold and use as a washcloth

Inactive ingredients

water

ANTISEPTIC WIPE

Contains 1 Single Use Wipe

Made In China

REORDER NO: 00-TOW-94185

Dist. By: Total Resources International Walnut, CA 91789

TOW

ANTISEPTIC WIPE
benzalkonium chloride patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55550-002
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g in 100 g

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC: 55550-002-88	1.6 g in 1 PACKET; Type 0: Not a Combination Product	08/01/2017	06/01/2019

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	08/01/2017	06/01/2019

Labeler - Total Resources International (790160535)

Registrant - Total Resources International (790160535)

Revised: 10/2019

Document Id: 962bc260-8759-2703-e053-2a95a90a260f

Set id: 576fc260-279e-5376-e053-2991aa0ac317

Version: 2

Effective Time: 20191030

Drug Labeling and Warnings

Drug Details [pdf]