NICE 'N CLEAN WIPES SANI-HANDS SANITIZING HAND WIPES

NICE N CLEAN WIPES SANI-HANDS SANITIZING HAND WIPES by

Drug Labeling and Warnings

NICE N CLEAN WIPES SANI-HANDS SANITIZING HAND WIPES by is a Otc medication manufactured, distributed, or labeled by Nice-Pak Products, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

NICE N CLEAN WIPES SANI-HANDS SANITIZING HAND WIPES- alcohol swab 
Nice-Pak Products, Inc.

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NICE 'N CLEAN WIPES SANI-HANDS SANITIZING HAND WIPES

Ethanol 70% by volume

Antiseptic

To decrease bacteria on the skin

Warnings

Flammable. Keep away from fire or flame.

For external use only.

When using this product avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.

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

Directions

Tear open packet.

Open and unfold wipe.

Thoroughly wipe hands, fingers and wrists using entire wipe.

Allow to dry.

For dirty hands, use first wipe to clean hands, then discard wipe; sanitize with second wipe

Discard after single use.

Water, Propylene Glycol, Glycerin, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate

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

Hand Sanitizing

Kills 99.99% of Bacteria*

Nice 'N Clean Wipes

From the makers of #1 Hand Wipe Brand in Health Care

SANI-HANDS SANITIZING HAND WIPES

70% ALCOHOL

1 HAND WIPE

Manufactured for:

Nice-Pak Products, Inc.

2 Nice-Pak Park

Orangeburg, NY 10962

Sani-Hands is a registered trademark of PDI. Nice 'n Clean (R) is a registered trademark of Nice-Pak Products, Inc.

*Kills 99.99% of commonly found bacteria

Based on GHX data 3rd Quarter 2020 for Sani-Hands(R) Instant Hand Sanitizing use

Made in USA with Domestic and Imported Materials

Not for individual sale

NDC: 44385-7022-1, 1 count packet, 2AH0078PAC:

Packette

NDC: 44285-7022-2, 24 count box - 5OH0078BX:

Carton

NICE N CLEAN WIPES SANI-HANDS SANITIZING HAND WIPES 
alcohol swab
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 44385-7022
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.7 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
GLYCERIN (UNII: PDC6A3C0OX)  
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 44385-7022-13.51 mL in 1 PACKET; Type 0: Not a Combination Product03/22/2021
2NDC: 44385-7022-224 in 1 BOX03/22/2021
2NDC: 44385-7022-13.51 mL in 1 PACKET; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)03/22/202111/08/2024
Labeler - Nice-Pak Products, Inc. (003778198)
Registrant - Nice-Pak Products, Inc. (003778198)

Revised: 11/2024
Document Id: 266e7fff-40b7-7a39-e063-6294a90a4c98
Set id: bdd462de-e6ed-52b6-e053-2995a90a17e0
Version: 8
Effective Time: 20241108