ISOPROPYL ALCOHOL liquid

Isopropyl Alcohol by

Drug Labeling and Warnings

Isopropyl Alcohol by is a Otc medication manufactured, distributed, or labeled by BuckAirways Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Isopropyl Alcohol 70%...................................................First aid antiseptic

Uses

helps prevent risk of infection from:

• minor cuts
• burns
• lacerations
• burns

Warnings

For External use only. Internal ingestion will result in gastric problems.

Flammable

• keep away from fire, flame, spark, heat, electric

Ask a doctor before use

for deep lacerations, puncture wounds, animal bites, or any serious burns

When using this product

• avoid from contact with eyes
• do not apply over large areas of body
• do not use longer than 1 week unless instructed by a physician

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 immediately.

Caution

Fumes created by Isopropyl Alcohol can be irritating to skin, eyes, or respiratory system. Do not apply if irritation is present on skin or continued irritation develops. Avoid from applying to eyes or mucous membranes. Do not inhale this product.

Directions

• clean the affected area
• apply a small amount of product on the area 1 to 3 times each day
• may be covered with a sterile
• bandage following application
• let dry prior to being bandaged

Other Information

• does not contain, nor is intended as a substitute for grain or ethyl alcohol

Inactive Ingredient

water

PRINCIPAL DISPLAY PANEL

75396-070-17 LABEL PANEL

75396-070-19 LABEL PANEL

INGREDIENTS AND APPEARANCE

ISOPROPYL ALCOHOL 
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75396-070
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: 75396-070-17	3785 mL in 1 JUG; Type 0: Not a Combination Product	07/18/2020
2	NDC: 75396-070-19	473 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/12/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/17/2020

Labeler - BuckAirways Inc. (117488255)

Registrant - BuckAirways Inc. (117488255)

Establishment
Name	Address	ID/FEI	Business Operations
BuckAirways Inc.		117488255	manufacture(75396-070)