DrugCite

ISOPROPYL RUBBING ALCOHOL 70% WITH WINTERGREEN - 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), Methyl Salicylate, FD&C Blue #1, FD&C Yellow #5

PRINCIPAL DISPLAY PANEL

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

PRINCIPAL DISPLAY PANEL


ISOPROPYL RUBBING ALCOHOL 70% WITH WINTERGREEN 
isopropyl alcohol  liquid
Product Information
Product Type HUMAN OTC DRUG NDC Product Code (Source) 52000-011
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  
METHYL SALICYLATE  
FD&C BLUE NO. 1  
FD&C YELLOW NO. 5  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 52000-011-01 118 mL In 1 BOTTLE, PLASTIC None
2 52000-011-02 177 mL In 1 BOTTLE, PLASTIC None
3 52000-011-03 237 mL In 1 BOTTLE, PLASTIC None
4 52000-011-04 296 mL In 1 BOTTLE, PLASTIC None
5 52000-011-05 355 mL In 1 BOTTLE, PLASTIC None
6 52000-011-06 414 mL In 1 BOTTLE, PLASTIC None
7 52000-011-07 473 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