WET NAP ANTIBACTERIAL HAND WIPES FRESH- antibacterial hand wipes swab

Wet Nap Antibacterial Hand Wipes Fresh by

Drug Labeling and Warnings

Wet Nap Antibacterial Hand Wipes Fresh by is a Otc medication manufactured, distributed, or labeled by Nice-Pak Products Inc, Tongling Jieya Biologic Technology Stock Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient

Benzalkonium chloride 0.13% w/w

PURPOSE

Purpose

Antiseptic handwash

INDICATIONS & USAGE

Use

For handwashing to decrease bacteria on the skin

WARNINGS

Warnings

For external use only

Keep out of reach of children

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

Do not use in the eyes

Discontinue use if irritation and redness develop.

If condition persists for more than 72 hours consult a doctor.

DOSAGE & ADMINISTRATION

Directions

To dispense, lift cover, remove seal, pull center sheet from roll, twist to a point, feed through dispenser hole in cover.

Keep lid closed to prevent moisture loss.

Use as a part of your hand cleansing routine.

Rub product onto hands and allow to dry.

Discard after single use.

REFERENCES

Other information

Lot No. and Expiration Date. Can be found on canister.

INACTIVE INGREDIENT

Inactive ingredients

Purified Water, SD Alcohol 40, Sorbic Acid, PPG-2 Hydroxyethyl Cocamide, Disodium EDTA, Aloe Barbadensis Leaf Juice, Fragrance

PRINCIPAL DISPLAY PANEL

The Original

Wet-Nap

ANTIBACTERIAL

HAND WIPES

Moisturizes with Aloe

Kills 99.99% of Germs

Fresh Scent

40

Count 5.7 X 7.5 (14.5 X 19.05 cm)

INGREDIENTS AND APPEARANCE

WET NAP ANTIBACTERIAL HAND WIPES FRESH 
antibacterial hand wipes swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 44385-7011
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 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
SORBIC ACID (UNII: X045WJ989B)
PPG-2 HYDROXYETHYL COCAMIDE (UNII: 34N07GUJ3X)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 44385-7011-1	193.1 mL in 1 CANISTER; Type 0: Not a Combination Product	03/22/2019
2	NDC: 44385-7011-2	24 in 1 BOX	03/22/2019
2		4.4 mL in 1 PACKET; Type 0: Not a Combination Product
3	NDC: 44385-7011-3	20 in 1 CELLO PACK	03/22/2019
3		2.6 mL in 1 APPLICATOR; Type 0: Not a Combination Product
4	NDC: 44385-7011-4	30 in 1 BOX	03/22/2019
4		4.4 mL in 1 PACKET; Type 0: Not a Combination Product
5	NDC: 44385-7011-5	266 mL in 1 CANISTER; Type 0: Not a Combination Product	03/22/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/22/2019

Labeler - Nice-Pak Products Inc (003778198)

Establishment
Name	Address	ID/FEI	Business Operations
Nice-Pak Products Inc		003778198	manufacture(44385-7011)

Establishment
Name	Address	ID/FEI	Business Operations
Tongling Jieya Biologic Technology Stock Co., Ltd.		529736361	manufacture(44385-7011)