ULTRA DEFENSE SANI SMART HAND SANITIZING WIPES- benzalkonium chloride cloth

Ultra Defense Sani Smart Hand Sanitizing Wipes by

Drug Labeling and Warnings

Ultra Defense Sani Smart Hand Sanitizing Wipes by is a Otc medication manufactured, distributed, or labeled by K7 Design Group Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Benzalkonium Chloride 0.13%

Purpose

Antibacterial

Uses

• For hand sanitizing to decrease bactera on the skin.
• Apply topically to the skin to help prevent cross contamination.
• Recommended for repeated use.
• Dries in seconds.

Warnings

For external use only.

When using this product

do not use in or contact the eyes.

Stop use and ask a doctor if

too much skin irritation or sensitivity develops or increases.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

• Remove lid and discard seal from container.
• Pull wipe from center of roll and thread through opening in lid.
• Do not push finger through opening.
• Replace lid, pull wipe up, and then out at a 45º angle. The next wipe dispenses automatically.
• Close lid to retain moisture.

Other information

• Lot No. Manufacture date and Expiration date can be found on canister.

Inactive ingredients

Water, Phenoxyethanol, Ethyl Alcohol, DMDM Hydantoin, Glycerin, Propylene Glycol, Cocamidopropyl Betaine, Decyl glucoside, Aloe Barbadensis Leaf Extract

Company Information

YOU MAY REPORT A SERIOUS ADVERSE REACTION TO THIS PRODUCT TO REPORT REACTION, LLC, PO BOX 22, PLAINSBORO, NJ 08536

MANUFACTURED FOR & DISTRIBUTED BY K7 DESIGN GROUP INC. 2433 KNAPP STREET, BROOKLYN, NY 11235

Product Packaging - 70 COUNT

ULTRA DEFENSE

SANI+SMART

HAND

SANITIZING

WIPES

70 COUNT

COTTON SOFT WIPES

KILLS 99.99% OF GERMS

5.71 in x 8.07 in (14.5cm x 20.5cm)

INGREDIENTS AND APPEARANCE

ULTRA DEFENSE SANI SMART HAND SANITIZING WIPES 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74177-850
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 g

Inactive Ingredients
Ingredient Name	Strength
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
DMDM HYDANTOIN (UNII: BYR0546TOW)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ALCOHOL (UNII: 3K9958V90M)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74177-850-70	70 in 1 CANISTER	08/25/2020
1		191 g in 1 CANISTER; 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	08/25/2020

Labeler - K7 Design Group Inc. (080357784)