PSP GO ISOPROPRYL RUBBING- isopropyl alcohol liquid 
RW Consumer Products Ltd

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

----------

PSP GO! Isopropryl Rubbing Alcohol

Drug Facts

Active ingredient

Isopropyl alcohol 70%

Purpose

First Aid Antiseptic

Uses

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

Warnings

Flammable, keep away from fire or flame

For external use only.

Do not use

• in the eyes or apply over large areas of the body
• longer than 1 week unless directed by a doctor

Ask a doctor before use if you have

  • deep or puncture wounds
  • animal bites
  • serious burns

When using this product

  • do not shake the bottle
  • keep away from eyes and other mucous membranes
  • if eye contact occurs, rinse with plenty of water

Stop use and ask doctor

if the condition persists or gets worse

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center immediately. 

Directions

• Clean the affected area
• Apply a small amount of this product on the area 1 to 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 • Do not use if shrink band around cap is broken or missing

Inactive ingredient

water

Package Labeling:

Label

PSP GO ISOPROPRYL RUBBING 
isopropyl alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69612-003
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL700 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69612-003-03100 mL in 1 BOTTLE; Type 0: Not a Combination Product03/01/201802/28/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A03/01/201802/28/2024
Labeler - RW Consumer Products Ltd (245592118)

Revised: 6/2022
 
RW Consumer Products Ltd