SOLGREAT ISOPROPYL ALCOHOL- isopropyl alcohol liquid

SolGreat Isopropyl Alcohol by

Drug Labeling and Warnings

SolGreat Isopropyl Alcohol by is a Otc medication manufactured, distributed, or labeled by PANATURAL USA, INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active lngredient  

Isopropyl alcohol

Purpose 

First aid antiseptic

Uses

helps prevent the risk of infection in:

• minor cuts
• scrapes
• burns

Warnings  

For external use only

Flammable

• keep away from fire or flame, heat, spark, electrical

Ask a doctor before use for deep or puncture 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.

Stop use and ask a doctor if condition persists or gets worse.

Caution – Fumes can be acutely irritating to skin, eyes and the respiratory system. Do not apply to irritated skin or if excessive irritation

develops. Avoid getting into the eyes or on mucous membranes. Avoid inhaling this product

Directions

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

Keep out of reach of children.

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

Other information

• does not contain, nor is intended as a substitute for grain or ethyl alcohol.
• will produce serious gastric disturbances if taken internally

Inactive ingredient

water

Product Label

INGREDIENTS AND APPEARANCE

SOLGREAT ISOPROPYL ALCOHOL 
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73913-007
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: 73913-007-01	473 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/31/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/31/2020

Labeler - PANATURAL USA, INC. (029572239)