DrugCite

ALLURE ISOPROPYL RUBBING ALCOHOL  - isopropyl alcohol liquid 
Universal Distribution Center LLC

ALLURE ISOPROPYL RUBBING ALCOHOL

Active Ingredients

Isopropyl alcohol (50% 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 puncture wounds, animal bites or serious burns

When using this product

  • do not get into eyes
  • do not apply over large areas of 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 affected area
  • apply a 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
  • dose not contain, nor is intended as a substitute for grain or  ethyl alcohol
  • will produce serious gastric disturbance if taken internally

Inactive ingredient

purified water

PRINCIPAL DISPLAY PANEL

ALLURE ISOPROPYL RUBBING ALCOHOL
FIRST AID ANTISEPTIC
12 FL.OZ (355 mL)
PRINCIPAL DISPLAY PANEL




ALLURE ISOPROPYL RUBBING ALCOHOL 
isopropyl alcohol  liquid
Product Information
Product Type HUMAN OTC DRUG NDC Product Code (Source) 52000-001
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ISOPROPYL ALCOHOL (ISOPROPYL ALCOHOL) ISOPROPYL ALCOHOL 50 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 52000-001-01 118 mL In 1 BOTTLE, PLASTIC None
2 52000-001-02 177 mL In 1 BOTTLE, PLASTIC None
3 52000-001-03 237 mL In 1 BOTTLE, PLASTIC None
4 52000-001-04 296 mL In 1 BOTTLE, PLASTIC None
5 52000-001-05 355 mL In 1 BOTTLE, PLASTIC None
6 52000-001-06 414 mL In 1 BOTTLE, PLASTIC None
7 52000-001-07 473 mL In 1 BOTTLE, PLASTIC None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part333A 06/29/2012

Labeler -  Universal Distribution Center LLC (019180459)
Establishment
Name Address ID/FEI Operations
Anicare Pharmaceuticals Pvt. Ltd 916837425 manufacture
Revised: 06/2012 Universal Distribution Center LLC