MEDIFIRST ISOPROPYL ALCOHOL- isopropyl alcohol spray

MediFirst Isopropyl Alcohol by

Drug Labeling and Warnings

MediFirst Isopropyl Alcohol by is a Otc medication manufactured, distributed, or labeled by Unifirst First Aid Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Drug Facts

Active Ingredient

Isopropyl Alcohol 70.0%

Purpose

First aid antiseptic

Uses

First aid to help prevent infection in minor cuts, scrapes, and burns

WARNINGS

Warnings

For external use only.

Flammable keep away from fire or flame

Do not use

• near eyes or mucous membranes
• on deep or puncture wounds, animal bites, or serious burns consult a physician
• on large areas of the body
• for longer than one week unless directed by a doctor

Stop use and ask a doctor if

• condition persists or gets worse

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• clean affected area and spray 1 to 3 times daily
• if bandaged, lket dry first
• may be covered with a sterile bandage
• not to be used on children under 12 years of age

Inactive ingredient

purified water

Questions or Comments?

1-800-634-7680

Medi-First Isopropyl Alcohol Spray Label

MEDI-FIRST ®

Isopropyl Alcohol

Pump Spray

Isopropyl Alcohol 70%

Flammable, keep away from fire or flame.

If taken internally, serious gastric disturbance will result.

Store at room temperature

59°-86ºF (15º-30ºC)

2 FL OZ (59.1ML)

INGREDIENTS AND APPEARANCE

MEDIFIRST ISOPROPYL ALCOHOL 
isopropyl alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 47682-268
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	550.2 g  in 1 L

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 47682-268-06	0.118 L in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	04/12/2013	05/01/2018
2	NDC: 47682-268-02	0.0591 L in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	04/12/2013

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/12/2013

Labeler - Unifirst First Aid Corporation (832947092)