HAND SANITIZER- ethyl alcohol gel 
L. Perrigo Company

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.

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Perrigo Hand Sanitizer Drug Facts

Active ingredient

Ethyl alcohol 70% v/v

Purpose

Antimicrobial

Use

•
hand sanitizer to help reduce bacteria on the skin

Warnings

For external use only.

Flammable. Keep away from fire or flame.

When using this product

•
keep out of eyes. In case of contact with eyes, flush thoroughly with water
•
avoid contact with broken skin

Stop use and ask a doctor if

irritation or rash appears and lasts

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away (1-800-222-1222).

Directions

•
put enough product in your palm to cover hands and rub hands together briskly until dry
•
children under 6 years of age should be supervised when using this product

Other information

•
store at 20-25°C (68-77°F)
•
may discolor certain fabrics or surfaces

Inactive ingredients

water, isopropyl alcohol, triethanolamine, propylene glycol, acrylates/c10-30 alkyl acrylate crosspolymer, glycerin, fragrance, aloe barbadensis leaf juice, tocopheryl acetate

Questions?

1-800-719-9260

Package/Label Principal Display Panel

Antimicrobial

Hand Sanitizer

Skin Moisturizing

Decreases Germs

2 FL OZ (59 mL)

Hand Sanitizer Label
HAND SANITIZER 
ethyl alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0113-7077
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
WATER (UNII: 059QF0KO0R)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
TROLAMINE (UNII: 9O3K93S3TK)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
GLYCERIN (UNII: PDC6A3C0OX)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0113-7077-1659 mL in 1 BOTTLE; Type 0: Not a Combination Product04/10/202009/30/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A04/10/202009/30/2021
Labeler - L. Perrigo Company (006013346)

Revised: 7/2022
Document Id: 9b6db427-44c9-486e-baba-8e03e8ce2bfe
Set id: 46cef162-d28c-4c45-82ef-df91b7da22e8
Version: 2
Effective Time: 20220714
 
L. Perrigo Company