MEDI-FIRST ANTISEPTIC WIPES- benzalkonium chloride swab MEDI-FIRST PLUS ANTISEPTIC WIPES- benzalkonium chloride swab

Medi-First Plus Antiseptic Wipes by

Drug Labeling and Warnings

Medi-First Plus Antiseptic Wipes by is a Otc medication manufactured, distributed, or labeled by Unifirst First Aid Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient
Benzalkonium chloride 0.133% w/v

Purpose

First aid antiseptic

Uses

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

Warnings

Do not use

• in the eyes or over large areas of the body
• in case of deep or puncture woulds, animal bite or serious burns, consult a doctor
• longer than 1 week unless directed by a doctor

Stop use and ask a doctor if

• if the condition persists or gets worse

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 clean the affected area
• discard after use
• may be covered with a sterile bandage
• if bandaged, let dry first

Other information

• store at room temperature 59-86ºF (15-30ºC)
• tamper evident sealed packets
• do not use any open or torn packets

Inactive ingredients

sodium bicarbonate, water

Questions or comments?

1-800-634-7680

Medi-First Antiseptic Wipes Label

Medi-First®

Antiseptic Wipes

First aid to help prevent infection

in minor cuts, scrapes and burns

Product # 21471

20 extra large wipes per box

Medi-First Plus Antiseptic Wipes Label

Medi First ®

Plus

Antiseptic Wipes

Extra Large

Reorder # 103071

20 Wipes

INGREDIENTS AND APPEARANCE

MEDI-FIRST ANTISEPTIC WIPES 
benzalkonium chloride swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 47682-212
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.33 mg  in 1 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: 47682-212-12	10 in 1 BOX	08/21/2017
1	NDC: 47682-212-99	1.4 mL in 1 PACKET; Type 0: Not a Combination Product
2	NDC: 47682-212-71	20 in 1 BOX	08/21/2017
2		1.4 mL in 1 PACKET; Type 0: Not a Combination Product
3	NDC: 47682-212-33	100 in 1 BOX	08/21/2017
3		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 not final	part333A	08/21/2017

MEDI-FIRST PLUS ANTISEPTIC WIPES 
benzalkonium chloride swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 47682-030
Route of Administration	TOPICAL

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
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 47682-030-71	20 in 1 BOX	08/21/2017
1		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 not final	part333A	08/21/2017

Labeler - Unifirst First Aid Corporation (832947092)