WOUND WIPES- benzalkonium chloride swab

WOUND WIPES by

Drug Labeling and Warnings

WOUND WIPES by is a Otc medication manufactured, distributed, or labeled by HART Health. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzalkonium Chloride 0.13% w/w

Purpose

Topical Antiseptic

Uses

First aid topical antiseptic to help prevent infection in:

• minor cuts
• scrapes
• burns
• abrasions

Warnings

For external use only

FLAMMABLE keep away from heat and flame

Do not use

• in the eyes or apply over large portions of the body
• on serious burns
• on animal bites
• on deep or puncture wounds

Stop use and ask a doctor if

• symptoms last more than 72 hours
• redness, swelling, irritation, or pain occurs

Keep out of reach of children.

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

Directions

Adults and chldren 12 years of age and over:

• apply topically to the clean affected area 1 to 3 times daily
• when dry, may be covered with a sterile bandage
• if gets in eyes, flush thoroughly with water

Children under 12 years of age:

• ask a doctor

Inactive Ingredients

Alcohol, Purified Water

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

WOUND WIPES 
benzalkonium chloride swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50332-0043
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	.0013 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50332-0043-2	20 in 1 BOX	04/01/1974
1		1.4 g in 1 PACKET; Type 0: Not a Combination Product
2	NDC: 50332-0043-0	10 in 1 BOX	04/01/1974
2		1.4 g in 1 PACKET; Type 0: Not a Combination Product
3	NDC: 50332-0043-5	5 in 1 BOX	04/01/1974
3		1.4 g in 1 PACKET; Type 0: Not a Combination Product
4	NDC: 50332-0043-7	100 in 1 BOX	04/20/2016
4		1.4 g in 1 PACKET; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/01/1974

Labeler - HART Health (069560969)