HAND SANITIZER WIPES- alcohol cloth 
HANUL CO.,LTD

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

----------

Rico Hand Sanitizing Wipes 70%

Active Ingredient(s)

Ethyl Alcohol 70% Purpose: Antiseptic

Purpose

Antiseptic, Hand Sanitizer Wipes

Use

To decrease bacteria on the skin that could cause disease

Warnings

For external use only: hands

Flammable. Keep away from fire and flame.

When using this product

keep out of eyes. In case of contact with eyes, flush thoroughly with water.

avoid contact with broken skin

do not inhale or ingest

Stop Use and ask a doctor if

irritation or redness develops

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

Other information

do not store above 105ºF/40°C

may discolor some fabrics

harmful to wood finishes and plastics

Inactive ingredients

water, glycerin, hydrogen peroxide

Package Label - Principal Display Panel

NDC: 75214-501-50

RICO HAND SANITIZING WIPES

NON STERILE SOLUTION

70% ALCOHOL ANTISEPTIC

Decreasing bacteria on the skin that could cause disease

50 wipes

wipes dimension 6in. x 8 In (15cm x 20m)

80wipes

50wipes

20 wipes

HAND SANITIZER WIPES 
alcohol cloth
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75214-501
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX) 1.83 mL  in 100 mL
HYDROGEN PEROXIDE (UNII: BBX060AN9V) 0.002 mL  in 100 mL
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:75214-501-50334 mL in 1 PACKAGE; Type 0: Not a Combination Product03/30/2020
2NDC:75214-501-20134 mL in 1 PACKAGE; Type 0: Not a Combination Product03/30/2020
3NDC:75214-501-80534 mL in 1 PACKAGE; Type 0: Not a Combination Product03/30/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A03/30/2020
Labeler - HANUL CO.,LTD (557814370)
Establishment
NameAddressID/FEIBusiness Operations
HANUL CO.,LTD557814370manufacture(75214-501)

Revised: 1/2021
Document Id: b878f90e-0fc4-373c-e053-2a95a90a2594
Set id: a3424b96-74b0-21c4-e053-2a95a90ae7ea
Version: 5
Effective Time: 20210109
 
HANUL CO.,LTD