Pullio Hand Sanitizing Wipes Peppermint by NAICO Drug Facts

Pullio Hand Sanitizing Wipes Peppermint by

Drug Labeling and Warnings

Pullio Hand Sanitizing Wipes Peppermint by is a Otc medication manufactured, distributed, or labeled by NAICO. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PULLIO HAND SANITIZING WIPES PEPPERMINT- benzalkonium chloride liquid 
NAICO

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Drug Facts

ACTIVE INGREDIENT

Benzalkonium Chloride 0.1%

INACTIVE INGREDIENTS

Water, Glycerin, Sodium Benzoate, Ethylhexylglycerin, Polysorbate20, Disodium EDTA, Citric Acid, Tocopheryl Acetate, Fragrance

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
■ aviod 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, under the skin irritation and rashes

KEEP OUT OF REACH OF CHILDREN

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

Uses

■ 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 40C (104F)

PACKAGE LABEL: Pullio hand sanitizing wipes (peppermint) / 20ct

PACKAGE LABEL: Pullio hand sanitizing wipes (peppermint) / 60ct

PULLIO HAND SANITIZING WIPES PEPPERMINT 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75536-0007
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)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM BENZOATE (UNII: OJ245FE5EU)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75536-0007-1	125 g in 1 CONTAINER; Type 0: Not a Combination Product	06/01/2020	10/30/2020
2	NDC: 75536-0007-2	390 g in 1 CONTAINER; Type 0: Not a Combination Product	06/01/2020	10/30/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	06/01/2020	10/30/2020

Labeler - NAICO (694725335)

Registrant - NAICO (694725335)

Establishment
Name	Address	ID/FEI	Business Operations
NAICO		694725335	manufacture(75536-0007)

Revised: 1/2025

Document Id: 2b05977a-b818-4462-e063-6294a90a7b29

34390-5

Set id: 2804ebe5-7a72-4a2e-b532-829e280cfffc

Version: 2

Effective Time: 20250106