Isopropyl Alcohol description, usages, side effects, indications, overdosage, supplying and lots more!

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Isopropyl Alcohol

Phoenix Pharmaceutical Inc./ Clipper Distributing, Inc.

Isopropyl Alcohol 70%


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

NDC 57319-430-09Isopropyl Alcohol 70%FOR EXTERNAL USE ONLYKEEP OUT OF REACH OF CHILDREN   

NET CONTENTS:

3.785L (1 GALLON)

PHOENIXTM

PHARMACEUTICAL, INC.

Manufactured for:

Clipper Distributing Company, LLC

St. Joseph, MO 64507

For Veterinary Use Only

Scrub hands and arms with soap and water, rinse with water, then scrub with alcohol solution for disinfecting.

External Solution for use as a topical antiseptic. may also be used for temporary relief of minor muscular aches or pain due to overexertion and fatigue. Apply full strength directly to affected area, wet thoroughly and massage briskly to stimulate circulation.

Store at controlled room temperature between 15° and 30°C (59°-86°F).

Manufactured by:
Ameri-Pac Inc.
St. Joseph, MO 64502

Rev. 10-09

TAKE TIME OBSERVE LABEL DIRECTIONS

Trademarks are property of
Clipper Distributing Company, LLC

Active ingredient

ACTIVE INGREDIENT:

Isopropyl Alcohol ................ 70%

INERT INGREDIENT

Deionized Water ................. 30%
Total ................................. 100%

WARNING

For external use only. If taken internally, serious gastric disturbance will result. Avoid contact with eyes. In case of eye contact, flush thoroughly with water. Call a physician.

First Aid:

Induce vomiting or use stomach pump.

CAUTION

FLAMMABLE
KEEP AWAY FROM FIRE OR FLAME

KEEP CONTAINER CLOSED WHEN NOT IN USE

Isopropyl Alcohol

Isopropyl Alcohol

Isopropyl Alcohol LIQUID

Product Information

Product Type Otc animal drug label Item Code (Source) NDC:57319-430
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
ISOPROPYL ALCOHOL ISOPROPYL ALCOHOL 70 mL

Inactive Ingredients

Ingredient Name Strength
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:57319-430-22 946 in 1 BOTTLE
2 NDC:57319-430-09 3785 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2002-01-29


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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