NOVITA ISOPROPYL RUBBING ALCOHOL- isopropyl alcohol liquid

NOVITA ISOPROPYL RUBBING ALCOHOL by

Drug Labeling and Warnings

NOVITA ISOPROPYL RUBBING ALCOHOL by is a Otc medication manufactured, distributed, or labeled by Shield Line LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DRUG FACTS

Isopropyl Alcohol 70% (v/v)

Purpose

First Aid Antiseptic

Uses

first aid to prevent the risk of infection in

• minor cuts
• scrapes
• burns

Warnings

For external use only

• Flammable, Keep away from fire and flame
• if taken internally, serious gastric disturbances will result

Ask a doctor before use if you have

• deep or puncture wounds
• animal bites
• serious burns

When using this product

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

STOP USE

Stop use and ask a doctor if

• condition persists or gets worse

Keep out of reach of children

If swallowed, get medical table or contact a Poison Control Center immediately

Directions

• clean the affected area
• apply a small amount of this product on the area 1 to 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 substitute for grain or ethyl alcohol

Inactive Ingredient

water

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

NOVITA ISOPROPYL RUBBING ALCOHOL 
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52410-1060
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 mL  in 100 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52410-1060-4	355 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/24/2016
2	NDC: 52410-1060-6	475 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/24/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	08/24/2016

Labeler - Shield Line LLC (078518916)