DrugCite

ISOPROPYL RUBBING ALCOHOL 70% - isopropyl alcohol liquid 
Universal Distribution Center LLC

Active Ingredients (by volume)

Isopropyl alcohol (70% conc.)

Purpose

First aid antiseptic

Uses

  • first aid to help prevent the risk of infection in minor cuts, scrapes and burns

Warnings

For external use only; flammable, keep away from fire or flame, heat, spark, electrical

Ask a doctor before use if you have

  • deep punctured 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 unless directed by a doctor

Stop using this product if

  • condition persists or gets worse

Keep this and all drugs out of the reach of children

In case of accidental ingestion, seek professional assistance or contact a Poison control center (1-800-222-1212) immediately

Directions

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

Other information

  • store at room temperature
  • does not contain, nor is intended as a substitute for grain or ethyl alcohol
  • will produce serious gastric disturbance if taken internally

Inactive ingredient

Water(Aqua)

PRINCIPAL DISPLAY PANEL

ISOPROPYL RUBBING ALCOHOL 70%
FIRST AID ANTISEPTIC
12 FL.OZ (355 mL)

PRINCIPAL DISPLAY PANEL


ISOPROPYL RUBBING ALCOHOL 70% 
isopropyl alcohol  liquid
Product Information
Product Type HUMAN OTC DRUG NDC Product Code (Source) 52000-010
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ISOPROPYL ALCOHOL (ISOPROPYL ALCOHOL) ISOPROPYL ALCOHOL 70 mL  in 100 mL
Inactive Ingredients
Ingredient Name Strength
WATER  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 52000-010-01 118 mL In 1 BOTTLE, PLASTIC None
2 52000-010-02 177 mL In 1 BOTTLE, PLASTIC None
3 52000-010-03 237 mL In 1 BOTTLE, PLASTIC None
4 52000-010-04 296 mL In 1 BOTTLE, PLASTIC None
5 52000-010-05 355 mL In 1 BOTTLE, PLASTIC None
6 52000-010-06 414 mL In 1 BOTTLE, PLASTIC None
7 52000-010-07 473 mL In 1 BOTTLE, PLASTIC None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333A 03/15/2012

Labeler -  Universal Distribution Center LLC (019180459)
Registrant - Anicare Pharmaceuticals Pvt. Ltd (916837425)
Establishment
Name Address ID/FEI Operations
Anicare Pharmaceuticals Pvt. Ltd 916837425 manufacture
Revised: 03/2013 Universal Distribution Center LLC