HAND SANITIZER  CIRCLE K- alcohol gel 
Lil' Drug Store Products, Inc

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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Hand Sanitizer
Circle K®

Drug Facts

Active ingredient

Ethyl alcohol 70%

Purpose

Antiseptic

Uses

  • to decrease bacteria on the skin that could cause disease
  • recommended for repeated use

Warnings

For external use only: hands

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
  • 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 (1-800-222-1222) right away.

Directions

  • wet hands thoroughly with product and allow to dry without wiping
  • for children under 6, use only under adult supervision
  • not recommended for infants

Other information

  • do not store above 105°F
  • may discolor some fabrics
  • harmful to wood finishes and plastics

Inactive ingredients

acrylates/C10-C30 alkyl acrylate crosspolymer, aloe barbadensis leaf juice, aminomethyl propanol, glycerin, maltodextrin, propylene glycol, water

Questions?

1-877-507-6516 (M-F 8AM-4:30PM CST)

Proudly distributed by Circle K Stores Inc.

PRINCIPAL DISPLAY PANEL - 59 mL Bottle Label

CIRCLE K®

Hand
Sanitizer

Kills more than
99.99% of
Germs*

2 FL OZ (59 mL)

Principal Display Panel - 59 mL Bottle Label
HAND SANITIZER   CIRCLE K
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66715-5761
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 (Allyl sucrose crosslinked) (UNII: 59TL3WG5CO)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
Glycerin (UNII: PDC6A3C0OX)  
Maltodextrin (UNII: 7CVR7L4A2D)  
Propylene Glycol (UNII: 6DC9Q167V3)  
Water (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:66715-5761-459 mL in 1 BOTTLE; Type 0: Not a Combination Product02/15/201903/25/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart333E11/01/201403/25/2023
Labeler - Lil' Drug Store Products, Inc (093103646)

Revised: 4/2020
Document Id: 7070301c-97fc-40a9-9b67-9ac088e25a62
Set id: 26d429b1-8c78-4843-9565-618ddd648736
Version: 3
Effective Time: 20200401
 
Lil' Drug Store Products, Inc