MEDI WIPER HAND SANITIZING WIPES- benzalkonium chloride liquid

Medi wiper Hand Sanitizing Wipes by

Drug Labeling and Warnings

Medi wiper Hand Sanitizing Wipes by is a Otc medication manufactured, distributed, or labeled by Timk Inc., NAICO. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzalkonium Chloride 0.1%

Inactive ingredients

Water, Phenoxyethanol, Glycerin, Sodium Benzoate, Polysorbate 20, Disodium EDTA, Tocopheryl Acetate, Citric Acid

Purpose

Antiseptic

Warnings

For external use only

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Stop use and ask a doctor if
■ hypersensitivity symptoms such as erythema, itching and dermatitis happen
■ skin irritation happens

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Do not use
■ in combination with soap or antibacterial cleansing agents
■ the product for a long time in the same area as swelling, inflammation or sickness may occur due to absorption through the skin

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When using this product
■ avoid using repeatedly in the same area, skin irritation may occur
■ avoid getting into the eyes (if contact occurs, wash well with clean water)
■ if following abnormal symptoms persist, discontinue use: Irritation around the eyes, ears, mucous membranes, including the mouth, skin irritation and rashes

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Keep out of reach of children
■ If swallowed, get medical help or contact a Poison Control Center right away

Keep out of reach of children

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

Use

■ Instant hand antiseptic to decrease bacteria on the skin

Directions

■ Clean with wipes and let dry
■ Do not flush

Other information

■ Read the directions and warnings before use
■ Avoid freezing and excessive heat above 40°C (104°F)

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MEDI WIPER HAND SANITIZING WIPES 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83930-010
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.1 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM BENZOATE (UNII: OJ245FE5EU)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83930-010-02	108 g in 1 CONTAINER; Type 0: Not a Combination Product	12/01/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	12/01/2024

Labeler - Timk Inc. (121537031)

Registrant - Timk Inc. (121537031)

Establishment
Name	Address	ID/FEI	Business Operations
NAICO		694725335	manufacture(83930-010)