ISOPROPYL RUBBING ALCOHOL- isopropyl alcohol liquid

Isopropyl Rubbing Alcohol by

Drug Labeling and Warnings

Isopropyl Rubbing Alcohol by is a Otc medication manufactured, distributed, or labeled by Strategic Sourcing Services LLC, Pharma Nobis, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Foster & Thrive Isopropyl Alcohol 70% USP

Active Ingredient

Isopropyl Alcohol 70% U.S.P. by volume

Purpose

First Aid Antiseptic

Uses

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

Warnings

For External use only.

USE IN WELL VENTILATED AREA. FUMES MAY BE HARMFUL.

Do not use

in the eyes or apply over a large area of the body when used as an antiseptic.

In case of

deep or puncture wounds, animal bites, or serious burns, consult a doctor.

When using this product:

• Do not apply to irritated skin and avoid getting into eyes or mucous membranes.
  

Stop use and consult a doctor

• if the condition persists or gets worse. Do not use longer than 1 week unless directed by a doctor.
• Discontinue use if excessive irritation of the skin develops.
  

Keep out of reach of children.

In case of accidental overdose, seek professional assistance or contact a Poison Control Center immediately. (1-800-222-1222)

Directions

For antiseptic use:  Apply a small amount of this product to the affected area 1 to 3 times daily.  May be covered with sterile bandage.  If bandaged let dry first.

For rubbing or massage use:  Apply compound externally on body until liquid has been absorbed or has been evaporated.

Inactive Ingredient:

Purified Water

Other Information:

FLAMMABLE:  Keep away from spark, heat and flame.

NOTICE:  This product does not contain eithyl or grain alcohol and is not sold as a substitute for preparations containing ethyl or grain alcohol.

Foster & Thrive Isopropyl Alcohol 70% USP 128oz (49348-030-40)

INGREDIENTS AND APPEARANCE

ISOPROPYL RUBBING ALCOHOL 
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70677-1207
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 L  in 100 L

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70677-1207-2	3.8 L in 1 BOTTLE; Type 0: Not a Combination Product	09/14/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	09/14/2024

Labeler - Strategic Sourcing Services LLC (116956644)

Registrant - Pharma Nobis, LLC (118564114)

Establishment
Name	Address	ID/FEI	Business Operations
Pharma Nobis, LLC		118564114	analysis(70677-1207) , manufacture(70677-1207) , pack(70677-1207) , label(70677-1207)