Fiori Hand Sanitizer by International Merchandise Group / distribuidora Cuscatlan

Fiori Hand Sanitizer by

Drug Labeling and Warnings

Fiori Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by International Merchandise Group, distribuidora Cuscatlan. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

FIORI HAND SANITIZER- alcohol gel 
International Merchandise Group

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.

----------

Warnings

Keep out of reach of children

Do not store above 105 f maydiscolor some fabrics. Harmful to wood finishes and plastics

Flammable keep away from fire or flame.

AVOID CONTACT WITH BROKEN SKIN. dO NOT INHALE OR INGEST. sTOP USE AND A DOCTOR IF IRRITATION AND REDNESS APPEARS OR IF CONDITION PERSISTS FOR MORE THEN 72 HOURS

DESCRIPTION

HAND SANITIZER

PURPOSE

TO DECREASE BACTERIAS ON THE SKIN THAT COULD CAUSE DISEASES RECOMENDED FOR REPEATED USE.

INACTIVE INGREDIENTS

Aqua/Water, Acrylates/ c10-30 ALkyl Acrylate Crosspolymer,Carbomer

Aminomethylpropanol

DIRECTIONS

WET HANDS THOROUGHLY WITH PRODUCT AND ALLOW TO DRY WITHOU WIPING. FOR CHILDREN UNDER 6 USE ONLY UNDER ADULT SUPERVISION. NOT RECOMENDED FOR INFANTS

Alcohol

Ethyl 70 %

Administration

For hands external use only

Wet hands throughly with product and allow to dry withou wiping .

For children under six use only under adult supervision. not recomended for infants

Indications and usage

For External use only

To decrease bacterias on the skin that could cause disease. Recomended for repeated use.

Warnings

Do Not store above 105 fmay discolor some fabrics. Harmful to wood fishes and plastics.

For External use only

flammable keep away from fire or flame

keep out of reach of children

Warning Section

Flammable keep away from fire or flame

active ingredient

ethyl Alcohol

Front Label

Back LabelFront Label

FIORI HAND SANITIZER 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 73971-191
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
CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)  
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 73971-191-93251 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product07/16/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A07/16/202012/31/2021
Labeler - International Merchandise Group (555630446)
Establishment
NameAddressID/FEIBusiness Operations
International Merchandise Group555630446label(73971-191)
Establishment
NameAddressID/FEIBusiness Operations
distribuidora Cuscatlan851247924manufacture(73971-191)

Revised: 1/2022
Document Id: d64cef5f-4072-4147-e053-2a95a90a3e43
Set id: aa92eeaa-1808-256e-e053-2a95a90a75cc
Version: 5
Effective Time: 20220123