ALCOHOL- isopropyl alcohol liquid

Alcohol by

Drug Labeling and Warnings

Alcohol by is a Otc medication manufactured, distributed, or labeled by Dynarex Corporation, Blossom Pharmaceuticals. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient                                       Purpose

Isopropyl Alcohol 70% v/v                         Antiseptic

PURPOSE

First aid to help 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.
• Not for use with electrocautinary devices or procedures
• Ask a doctor before use if you have deep puncture wounds, animal bites or serious burns.
• Stop use and ask a doctor if condition persist or gets worse.

For rubbing and massaging:

• Caution: Do not apply to irritated skinor if excessive irritation develops
• Avoid getting into eyes or mucous membranes

INDICATIONS & USAGE

When using this product:

• do not get in eyes
• do not apply over large areas of the body
• do not use longer than 1 week unless directed by a doctor

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

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

DOSAGE & ADMINISTRATION

DIRECTIONS:

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

OTHER INFORMATION

• Store at room temperature: 15 deg C to 30 deg C   59 deg F to 86 deg F
• avoid excessive heat
• Does not contain, nor is it intended as a substitute for grain or ethyl alcohol
• Will produce serious gastric disturbances if taken internally

INACTIVE INGREDIENT

Inactive Ingredient

• Water
  

PRINCIPAL DISPLAY PANEL

DYNAREX 70% ISOPROPYL ALCOHOL

70 IPA.jpg

INGREDIENTS AND APPEARANCE

ALCOHOL 
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 67777-304
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	0.7 mL  in 1 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 67777-304-01	473 mL in 1 BOTTLE
2	NDC: 67777-304-02	295 mL in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/29/2014

Labeler - Dynarex Corporation (008124539)

Registrant - Dynarex Corporation (008124539)

Establishment
Name	Address	ID/FEI	Business Operations
Blossom Pharmaceuticals		677381470	manufacture(67777-304)