TRIP WIPES- benzalkonium chloride cloth

Trip Wipes by

Drug Labeling and Warnings

Trip Wipes by is a Otc medication manufactured, distributed, or labeled by DETROIT WICK, Precare Corp. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Benzalkonium chloride 0.13%

Purpose

Antimicrobial

Uses

• For hand sanitizing to decrease bacteria on the skin
• Recommended for repeated use

Warnings

For external use only

When using this product

avoid contact with eyes. In case of eye contact, flush eyes with water.

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.

Directions

• take wipe and rub thoroughly over all surfaces of both hands. Wet hands thoroughly with wipe
• rub hands together briskly to dry without wiping
• dispose of wipe
• do not flush

Other information

Store between 15°-30°C (59°F - 86°F).

Avoid freezing and excessive heat above 40°C (104°F)

Inactive ingredients

Purified Water, Aloe Barbadensis Leaf Extract, Citric Acid, Fragrance, Phenoxyethanol, Polysorbate 20, Potassium Sorbate, Sodium Benzoate, Vitamin E

Principal Display Panel

73030-025-01

ANTI-BACTERIAL WIPES

SMELLS AMAZING SOFTENS HANDS

10 BIG WIPES

KILLS 99.9% OF GERMS

DO NOT FLUSH

INGREDIENTS AND APPEARANCE

TRIP WIPES 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73030-025
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)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
SODIUM BENZOATE (UNII: OJ245FE5EU)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73030-025-01	10 in 1 BOX	12/13/2022
1		1 g 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	12/13/2022

Labeler - DETROIT WICK (061117661)

Registrant - Precare Corp (858442403)

Establishment
Name	Address	ID/FEI	Business Operations
Precare Corp		858442403	manufacture(73030-025)