ISOPROPYL ALCOHOL liquid

Isopropyl Alcohol by

Drug Labeling and Warnings

Isopropyl Alcohol by is a Otc medication manufactured, distributed, or labeled by Medical Chemical Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PURPOSE

Antiseptic

INDICATIONS & USAGE

Directions: Apply to affected area for first-aid treatment of minor cuts and abrasions.  In case of deep or puncture wounds consult a physician.  Discontinue use and get medical aid if redness, irritation or infection develops.  Apply liberally for rubbing.

ACTIVE INGREDIENT

Active ingredient:  Isopropyl alcohol, 70%

KEEP OUT OF REACH OF CHILDREN

Warnings:  For external use only.  Avoid contact with eyes or mucous membranes.  Ingestion will result in gastrointestinal distress, unconsciousness and death.  Keep out of reach of children.  In case of ingestion contact a poison control center immediately.

USER SAFETY WARNINGS

Flammable: Avoid sources of ignition.  Do not use around open flames.

WARNINGS

Warnings:  For external use only.  Avoid contact with eyes or mucous membranes.  Ingestion will result in gastrointestinal distress, unconsciousness and death.  Keep out of reach of children.  In case of ingestion contact a poison control center immediately.

INACTIVE INGREDIENT

Inactive Ingredients: Water

DOSAGE & ADMINISTRATION

Directions:  Apply to affected area for first-aid treatment of minor cuts and abrasions.  In case of deep or puncture wounds consult a physician.  Discontinue use and get medical aid if redness, irritation or infection develops.  Apply liberally for rubbing.

PRINCIPAL DISPLAY PANEL

ipa70label.jpg

INGREDIENTS AND APPEARANCE

ISOPROPYL ALCOHOL 
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 12745-105
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	70.14 g  in 100 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 12745-105-01	946 mL in 1 BOTTLE, PLASTIC; Type 1: Convenience Kit of Co-Package	06/15/1954
2	NDC: 12745-105-02	3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/15/1954
3	NDC: 12745-105-03	3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/15/1954
4	NDC: 12745-105-04	3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/15/1954
5	NDC: 12745-105-05	18927 mL in 1 CONTAINER; Type 0: Not a Combination Product	06/15/1954
6	NDC: 12745-105-06	18927 mL in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK; Type 0: Not a Combination Product	06/15/1954
7	NDC: 12745-105-07	208198 mL in 1 DRUM; Type 0: Not a Combination Product	06/15/1954

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part344	06/15/1954

Labeler - Medical Chemical Corporation (008496861)

Establishment
Name	Address	ID/FEI	Business Operations
Medical Chemical Corporation		008496861	manufacture(12745-105)