Dr. Lift Isopropyl Alcohol

Dr. Lift Isopropyl Alcohol by

Drug Labeling and Warnings

Dr. Lift Isopropyl Alcohol by is a Otc medication manufactured, distributed, or labeled by Spa de Soleil, Spa de Soleil, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DR. LIFT ISOPROPYL ALCOHOL- isopropyl alcohol solution 
Spa de Soleil

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.

----------

Dr. Lift Isopropyl 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, burns.

Warnings For external use only

Flammable

  • Keep away from fire or flame, heat, spark, electrical. Flash point 72°F.
  • do not use with eletocautery procedures.

Ask a doctor before use if you have deep or puncture 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 1 week unless directed by a doctor

Stop use and ask a doctor if condition persists or gets worse

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

<Directions clean the affected area. apply 1 to 3 times daily.

Other information does not contain, nor is intended as a substitue for grain or ethyl alcohol. will produce serious gastric disturbances if taken internally.

Inactive Ingredient purified water

Principal Display Panel

Dr_LIFT_IPA_70.jpg

DR. LIFT ISOPROPYL ALCOHOL 
isopropyl alcohol solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 68062-2252
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL660 mL  in 943 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 68062-2252-1943 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A12/01/202001/08/2023
Labeler - Spa de Soleil (874682867)
Establishment
NameAddressID/FEIBusiness Operations
Spa de Soleil, Inc.874682867manufacture(68062-2252)

Revised: 1/2023
 

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.