REDIWIPES ANTISEPTIC CLEANING TOWELETTES- bzk antiseptic wipes swab

Rediwipes Antiseptic Cleaning Towelettes by

Drug Labeling and Warnings

Rediwipes Antiseptic Cleaning Towelettes by is a Otc medication manufactured, distributed, or labeled by Redicare LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients...................................Uses

Benzalkonium Chloride 0.13%................................First Aid Antiseptic

Uses:

Antiseptic cleansing of face, hands and body to decrease bacteria on skin without soap and water. Antiseptic to help prevent further infection in minor cuts, scrapes, and burns.

Warnings

For external use only.

Do not use:

• In the eyes. If this happens, rinse thoroughly with water.
• Over large areas of the body
• Longer than 1 week unless directed by a doctor

Stop use and ask doctor if:

• Irritation of redness develop and persists for more than 72 hours.
• 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.

Ask a doctor before use if you have:

• Deep or puncture wounds
• Animal bites
• Serious burns

Directions:

Tear open packet, unfold and use as a washcloth. Allow hands to dry without wiping.

Inactive Ingredients:

purified water, sodium bicarbonate

Other information:

• For external use only.
• Store at room temperature
• Do not use if packet is torn or opened

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

REDIWIPES ANTISEPTIC CLEANING TOWELETTES 
bzk antiseptic wipes swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71105-323
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 g

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: 71105-323-03	1 in 1 BOX	03/31/2017
1	NDC: 71105-323-02	25 in 1 PACKET
1	NDC: 71105-323-01	1.5 g in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/31/2017

Labeler - Redicare LLC (800149346)