Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

First Aid Antiseptic

Use(s)

First aid to help prevent skin infection in minor cuts, scrapes, and burns.

Warnings

For External Use Only

Do not use:

• As an antiseptic for more than 1 week

• In the eyes

Ask a doctor before use if you have

Deep or puncture wounds, animal bites, or serious burns.

Stop use and ask a doctor if

• Irritation and redness develop

• Condition persists or gets worse

Keep Out Of Reach Of Children.

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

• Clean the affected area.

• May be covered with a sterile bandage.

• If bandaged, let dry first.

Other Information

• Store at room temperature 15º-30ºC (59º-86ºF).

• Avoid excessive heat.

• Tamper Evident. Do not use if packet is torn or cut.

Inactive ingredients

Water

Questions?

1-888-DYNAREX Monday - Friday, 9AM - 5PM EST

Label

1303 BX MNFL010 1303 Label

Label

1303 BX MASTER

Label

1331 MC MASTER 1331

Label

1332 BX MASTER 1332

Label

1333 BX MASTER 1333

Label

1331 MC MNFL010

Label 1303UB-10

1303UB-10_BX_MASTER 1303UB-10

Label 1303-40

1303-40_BX_MASTER 1303-40

Label 1333-50

1333-50_BX_MASTER 1333-50

BZK PADS
benzalkonium chloride swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:67777-245
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg in 1 mL

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

Product Characteristics
Color		Score
Shape	RECTANGLE	Size
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:67777-245-11	10000 in 1 CASE	04/05/2011
1	NDC:67777-245-01	100 in 1 BOX
1		0.55 mL in 1 PACKET; Type 0: Not a Combination Product
2	NDC:67777-245-02	1000 in 1 BOX	03/30/2017
2		0.55 mL in 1 PACKET; Type 0: Not a Combination Product
3	NDC:67777-245-04	1000 in 1 CASE	04/05/2011
3	NDC:67777-245-14	10 in 1 BOX
3		0.55 mL in 1 PACKET; Type 0: Not a Combination Product
4	NDC:67777-245-05	750 in 1 CASE	04/05/2011
4	NDC:67777-245-15	25 in 1 BOX
4		0.55 mL in 1 PACKET; Type 0: Not a Combination Product
5	NDC:67777-245-16	1000 in 1 CASE	04/05/2011
5	NDC:67777-245-06	10 in 1 BOX
5		0.55 mL in 1 PACKET; Type 0: Not a Combination Product
6	NDC:67777-245-18	1000 in 1 CASE	04/05/2011
6	NDC:67777-245-08	40 in 1 BOX
6		0.55 mL in 1 PACKET; Type 0: Not a Combination Product
7	NDC:67777-245-17	1000 in 1 CASE	04/05/2011
7	NDC:67777-245-07	50 in 1 BOX
7		0.55 mL in 1 PACKET; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M003	04/05/2011

Labeler - Dynarex Corporation (008124539)

Registrant - Dynarex Corporation (008124539)