Done Hand Sanitizer Gel - Isopropyl Alcohol 75%

Done Hand Sanitizer- Isopropyl Alcohol by

Drug Labeling and Warnings

Done Hand Sanitizer- Isopropyl 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- ISOPROPYL ALCOHOL- isopropyl alcohol liquid 
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 Gel - Isopropyl Alcohol 75%

Drug Facts

Active Ingredient

Isopropyl Alcohol 75%

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:

Bottle

DONE HAND SANITIZER- ISOPROPYL ALCOHOL 
isopropyl alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 77142-012
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL0.75 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: 77142-012-003785 mL in 1 BOTTLE; Type 0: Not a Combination Product08/31/202010/14/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E08/31/202010/14/2021
Labeler - Olein Recovery Corporation (188543446)

Revised: 10/2022
Document Id: ebda7260-d8cd-21d3-e053-2995a90a3982
Set id: be2fa90a-2360-413e-bdbd-737c521ffd4c
Version: 3
Effective Time: 20221025