XTRAGUARD ANTIBACTERIAL HAND WIPES- benzalkonium chloride swab

Xtraguard Antibacterial Hand Wipes by

Drug Labeling and Warnings

Xtraguard Antibacterial Hand Wipes by is a Otc medication manufactured, distributed, or labeled by Munchkin Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DOSAGE & ADMINISTRATION

30 Wipes | 1 wipe: 8 in. x 4 in. (20.3 cm x 10.2 cm)

ACTIVE INGREDIENT

Benzalkonium Chloride 0.13% - Antimicrobial

PURPOSE

Antimicrobial

INDICATIONS & USAGE

Uses

• To sanitize hands and decrease bacteria on skin
• Recommended for repeated use

WARNINGS

Warnings

For external use only.

When using this product avoid contact with eyes. If contact occurs, wash using water and discontinue use.

Stop use and ask a doctor if irritation or redness develops or if condition persists for more than 72 hours.

Keep out of reach of children.

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

INSTRUCTIONS FOR USE

Directions

• Wet hands thoroughly with wipe.
• Allow to dry without wiping.
• Discard wipe in trash after use. Do not flush in toilet.

STORAGE AND HANDLING

Other information

• Keep away from direct sunlight. Store at room temperature.

INACTIVE INGREDIENT

Inactive ingredients

Water, Glycerin, Aloe Barbadensis Leaf Juice, Phenoxyethanol, Tocopheryl Acetate

PRINCIPAL DISPLAY PANEL

30 Wipes | NDC: 81725-614-01

PRINCIPAL DISPLAY PANEL

60 Wipes | NDC: 81725-614-10

PRINCIPAL DISPLAY PANEL

60 Wipes | NDC: 81725-614-20

PRINCIPAL DISPLAY PANEL

90 Wipes | NDC: 81725-614-15

PRINCIPAL DISPLAY PANEL

90 Wikpes | NDC: 81725-614-25

INGREDIENTS AND APPEARANCE

XTRAGUARD ANTIBACTERIAL HAND WIPES 
benzalkonium chloride swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81725-614(NDC:69821-001)
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
PHENOXYETHANOL (UNII: HIE492ZZ3T)	0.3 g  in 100 g
ALOE VERA LEAF (UNII: ZY81Z83H0X)	0.2 g  in 100 g
WATER (UNII: 059QF0KO0R)	98.27 g  in 100 g
GLYCERIN (UNII: PDC6A3C0OX)	1 g  in 100 g
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)	0.1 g  in 100 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81725-614-10	2 in 1 CARTON	05/26/2021
1		30 in 1 BAG
1		0.13 g in 1 POUCH; Type 0: Not a Combination Product
2	NDC: 81725-614-15	3 in 1 CARTON	05/26/2021
2		30 in 1 BAG
2		0.13 g in 1 POUCH; Type 0: Not a Combination Product
3	NDC: 81725-614-20	2 in 1 CARTON	05/26/2021
3		30 in 1 BAG
3		0.13 g in 1 POUCH; Type 0: Not a Combination Product
4	NDC: 81725-614-25	3 in 1 CARTON	05/26/2021
4		30 in 1 BAG
4		0.13 g in 1 POUCH; Type 0: Not a Combination Product
5	NDC: 81725-614-01	30 in 1 BAG	05/26/2021
5		0.13 g in 1 POUCH; 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	05/26/2021

Labeler - Munchkin Inc. (787026855)