BZK ANTISEPTIC SWAB- benzalkonium chloride swab 
Foshan Flying Medical Products Co., Ltd.

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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BZK antiseptic swab

DRUG FACTS

ACTIVE INGREDIENT

Benzalkonium chloride .13% w/v

PURPOSE

Antiseptic

USE

Antiseptic cleaning of face, hands and body without soap and water.

WARNINGS

For external use only. Flammable, keep away from fire or flame.

DO NOT USE, in the eyes or apply over large areas of the body.

STOP USE: If irritation, redness or other symptoms develop.

ASK A DOCTOR: If condition persists or gets worse.

CAUTION: Keep out of reach of children

If swallowed, get medical help or contact aPoisonControlCenterright away.

DIRECTIONS

Tear open packet, unfold and use as a washcloth.

OTHER INFORMATION

Store at room temperature.

INACTIVE INGREDIENTS

Purified water.

image of labeling

INACTIVE INGREDIENTS

Purified water

DIRECTIONS

Tear open packet, unfold and use as a washcloth.

WARNINGS

For external use only. Flammable, keep away from fire or flame.

DO NOT USE, in the eyes or apply over large areas of the body.

STOP USE: If irritation, redness or other symptoms develop.

ASK A DOCTOR: If condition persists or gets worse.

USE

Antiseptic cleaning of face, hands and body without soap and water.

CAUTION: Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away.

PURPOSE

Antiseptic

ACTIVE INGREDIENT

Benzalkonium chloride .13% w/v

image description

BZK ANTISEPTIC SWAB 
benzalkonium chloride swab
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:54429-0103
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1.3 mg  in 1 mL
Inactive Ingredients
Ingredient Name Strength
WATER (UNII: 059QF0KO0R)  
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:54429-0103-1 1.4 mL in 1 PACKET
2 NDC:54429-0103-2 1.4 mL in 1 PACKAGE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333A 12/27/2012
Labeler - Foshan Flying Medical Products Co., Ltd. (527021584)
Registrant - Foshan Flying Medical Products Co., Ltd. (527021584)
Establishment
Name Address ID/FEI Business Operations
Foshan Flying Medical Products Co., Ltd. 527021584 manufacture(54429-0103)

Revised: 5/2014
Document Id: 73271a51-448e-42b6-a49c-e8c5eeded43b
Set id: 9e51b2b5-e60d-4269-ac84-783576bade78
Version: 5
Effective Time: 20140522
 
Foshan Flying Medical Products Co., Ltd.