Done Hand Sanitizer Ethyl Alcohol

Done Hand Sanitizer Ethyl Alcohol by

Drug Labeling and Warnings

Done Hand Sanitizer Ethyl Alcohol by is a Otc medication manufactured, distributed, or labeled by Olein Recovery Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DONE HAND SANITIZER ETHYL ALCOHOL- alcohol gel 
Olein Recovery Corporation

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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Done Hand Sanitizer Ethyl Alcohol

Drug Facts

Active Ingredient

Ethyl Alcohol 80% v/v

Purpose

Antiseptic

Uses

Health care personnel hand rub to help reduce bacteria that potentially can cause disease.

Warnings

For external use only. Flammable, Keep away from heat or flame.

DO NOT USE

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

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

Directions

  • Place enough product on hands to cover all surfaces. Rub hands together until dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Other Information

  • Store between 59°-86°F)
  • Avoid freezing and excessive heat above 104°F

Inactive Ingredients

Carbomer, Water, fragrance

Package Labeling: 118 ml

Bottle2

DONE HAND SANITIZER ETHYL ALCOHOL 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 77142-002
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.8 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 77142-002-01118 mL in 1 BOTTLE; Type 0: Not a Combination Product04/21/202010/14/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E04/21/202010/14/2021
Labeler - Olein Recovery Corporation (188543446)

Revised: 11/2022
Document Id: ed0d8184-293c-6e1c-e053-2a95a90a6dda
Set id: 38beee38-4524-4446-b8ac-2406e14b7a44
Version: 3
Effective Time: 20221109