FIRST AID DIRECT ANTISEPTIC WIPE- benzalkonium chloride sponge

First Aid Direct Antiseptic Wipe by

Drug Labeling and Warnings

First Aid Direct Antiseptic Wipe by is a Otc medication manufactured, distributed, or labeled by Cintas Corporation, Changzhou Maokang Medical Products Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient (in each towelette)

Benzalkonium Chloride 0.133%

PURPOSE

Purpose

first aid antiseptic

INDICATIONS & USAGE

Uses

first aid to reduce bacteria in minor cuts, scrapes and burns

WARNINGS

Warnings

For external use only

Do not use

• in the eyes or apply over large areas of the body
• longer than 1 week unless directed by a doctor

Ask a doctor before use if you have

• deep or puncture wounds
• animal bites
• serious burns

Stop use and ask a doctor if

• condition persists or gets worse

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

DOSAGE & ADMINISTRATION

Directions

• tear open packet, unfold, use and discard
• clean the affected area
• maybe covered with a sterile bandage. If bandaged, let dry first.

OTHER SAFETY INFORMATION

Other information

• do not use if packet is torn, cut or opened
• store at room temperature

INACTIVE INGREDIENT

Inactive ingredients

purified water, sodium bicarbonate

QUESTIONS

Questions? 1-877-973-2811

Principal Display Panel

Antiseptic Wipe

One Wipe Saturated with Benzalkonium Chloride

EXTERNAL USE ONLY

INGREDIENTS AND APPEARANCE

FIRST AID DIRECT ANTISEPTIC WIPE 
benzalkonium chloride sponge

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 42961-127
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	.133 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 42961-127-02	10 in 1 BAG	09/28/2023
1	NDC: 42961-127-01	1.4 mL in 1 PACKET; Type 0: Not a Combination Product
2	NDC: 42961-127-03	100 in 1 BOX	09/28/2023
2	NDC: 42961-127-01	1.4 mL 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 Drug	M003	09/28/2023

Labeler - Cintas Corporation (056481716)

Establishment
Name	Address	ID/FEI	Business Operations
Changzhou Maokang Medical Products Co., Ltd.		421317073	manufacture(42961-127)