Done 70% Isopropyl Alcohol

Done 70 Isopropyl Alcohol by

Drug Labeling and Warnings

Done 70 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 70 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 70% Isopropyl Alcohol

Drug Facts

Active Ingredient (by volume)

Ispropyl Alcohol 70%

Purpose

first aid antiseptic

Uses

  • first aid to help prevent the risk of infection in minor cut, scrapes and burns

Warnings

For external use only

  • flammable, keep away from fire or flame
  • if taken internally serious gastric disturbances will result

Ask a doctor before use if you have

  • deep or punture wounds, animal bites or serious burns

WHen using this product

  • do not get into eyes
  • do not apply over large areas of the body
  • do not use longer than one week unless directed by a doctor

Stop use and ask doctor if

condition persists or gets worse

Keep out of reach of children.

In case of ingestion, get medical help or contact a Poison Control Center immediately.

Directions

  • clean affected area
  • apply small amount of this product on the area 1-3 times daily
  • if bandaged, let dry first
  • may be covered with a sterile bandage

Other information

  • store at room temperature
  • does not contain, nor is intended as a substitute for grain or ethyl alcohol

Inactive ingredient

purified water

Package Labeling: 295.7ml

Bottle2

DONE 70 ISOPROPYL ALCOHOL 
isopropyl alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 77142-011
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL0.7 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 77142-011-02295.7 mL in 1 BOTTLE; Type 0: Not a Combination Product05/15/202010/14/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E05/15/202010/14/2020
Labeler - Olein Recovery Corporation (188543446)

Revised: 11/2022
Document Id: ed735503-1d18-dde8-e053-2995a90ae448
Set id: aef38669-9195-41b5-e053-2a95a90a2519
Version: 2
Effective Time: 20221114