CRAZY AARONS HAND SANITIZER 68% ALCOHOL- alcohol hand sanitizer gel 
Crazy Aaron Enterprises, 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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Crazy Aarons Sea Ya Later Hand Sanitizer

Drug Facts

Drug Facts

Active Ingredient

Ethanol 68% v/v

Purpose

Antiseptic

Use

Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

For external use only.

Flammable - Keep away from fire or flame.

When using this product

keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if

irritation or rash occurs. These may be signs of a serious condition..

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away.

  • on open skin wounds
  • on children less than 2 months of age

Directions

• Place enough product on hands to cover all surfaces. Rub hands together briskly until dry.

• Supervise children under 6 years of age when using this product to avoid swallowing



Other information

Inactive Ingredients

Ammonium Polyacryloyldimethyl Taurate, Blue 1, Calcium Sodium Borosilicate, FD&C Yellow 5 Aluminum Lake, Fragrance, Glycerin, Mica, Propylene Glycol, Silica, Tin Oxide, Titanium Dioxide, Water

PDP-Drug Facts

CRAZY AARONS HAND SANITIZER 68% ALCOHOL 
alcohol hand sanitizer gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80032-300
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL68 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
FRAGRANCE CLEAN ORC0600327 (UNII: 329LCV5BTF)  
GLYCERIN (UNII: PDC6A3C0OX)  
WATER (UNII: 059QF0KO0R)  
AMMONIUM POLYACRYLOYLDIMETHYL TAURATE (55000 MPA.S) (UNII: F01RIY4371)  
HYDRATED SILICA (UNII: Y6O7T4G8P9)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
BOROSILICATE GLASS (UNII: BOJ6T9AR90)  
MICA (UNII: V8A1AW0880)  
DIBUTYLTIN OXIDE (UNII: T435H74FO0)  
COBALT TITANIUM OXIDE (UNII: CN422GY0TE)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
3-(NONYLOXY)1,2-PROPANEDIOL (UNII: 73E9M7IT67)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:80032-300-01118 mL in 1 BOTTLE; Type 0: Not a Combination Product08/20/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A08/20/2020
Labeler - Crazy Aaron Enterprises, Inc. (092666531)
Registrant - Crazy Aaron Enterprises, Inc. (092666531)
Establishment
NameAddressID/FEIBusiness Operations
B & J Group064604222manufacture(80032-300)
Establishment
NameAddressID/FEIBusiness Operations
Action-Pak, Inc.117537305relabel(80032-300) , repack(80032-300)

Revised: 9/2020
Document Id: afe83cd3-241f-7768-e053-2a95a90aa2d8
Set id: ad6386c9-cab6-3569-e053-2995a90addce
Version: 4
Effective Time: 20200922
 
Crazy Aaron Enterprises, Inc.