CIRCLE K HAND SANITIZER- 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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Circle K ® Hand Sanitizer, 1.25oz

Drug Facts

Active ingredient

Ethyl alcohol 62%

Purpose

Antiseptic

Uses

Warnings

For external use only: hands

Flammable. Keep away from heat 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 (1-800-222-1222) right away.

Directions

Other information

Inactive ingredients

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

Questions?

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

Proudly distributed by Circle K Stores Inc

PRINCIPAL DISPLAY PANEL - 37 mL Bottle Label

CIRCLE K ®

Hand
Sanitizer

Kills 99.99%
of Germs*

*Effective at eliminating 99.99% of
many common harmful germs and
bacteria in as little as 15 seconds.

1.25 FL OZ
(37 mL)

PRINCIPAL DISPLAY PANEL - 37 mL Bottle Label
CIRCLE K HAND SANITIZER 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66715-5863
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 mg  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
TROLAMINE (UNII: 9O3K93S3TK)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:66715-5863-237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/06/201701/28/2025
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E06/06/201701/28/2025
Labeler - Lil' Drug Store Products, Inc. (093103646)

Revised: 8/2022
Document Id: e78bd59c-6e73-75cc-e053-2995a90ae030
Set id: 044dd404-f1d6-499e-a102-d922107872cb
Version: 5
Effective Time: 20220831
 
Lil' Drug Store Products, Inc.