DONE 70 ISOPROPYL ALCOHOL- isopropyl alcohol liquid

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]

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: 236.5ml

Package Labeling: 295.7ml

Package Labeling: 354.8ml

Package Labeling: 946ml

Package Labeling: 3785.4ml

INGREDIENTS AND APPEARANCE

DONE 70 ISOPROPYL ALCOHOL 
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77142-011
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	0.7 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77142-011-01	236.5 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/15/2020
2	NDC: 77142-011-02	295.7 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/15/2020
3	NDC: 77142-011-03	354.8 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/15/2020
4	NDC: 77142-011-04	946 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/15/2020
5	NDC: 77142-011-05	3785.4 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/15/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	05/15/2020

Labeler - Olein Recovery Corporation (188543446)