MAXIM 70% ISOPROPYL RUBBING ALCOHOL- isopropyl alcohol liquid 
OSTL, INC.

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.

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maxim 70% ISOPROPYL RUBBING ALCOHOL

Drug Facts

Active ingredients (by volume)

Isopropyl alcohol (70% Conc)

Purpose

First aid antiseptic

Keep out of reach of children. If swallowed, get medical help or contact poison control centre right away. (1-800-222-1222)

Uses helps 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

Ask a doctor before use for deep or puncture wounds, animals bites or serious burns

When using this products • do not get into eyes • do not inhale • do not apply over large areas of the body • do not use longer than 1 week

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

Directions

•Clean affected area •spray a small amount of this product on the area 1 to 3 times daily •may be covered with sterile bandage
•if bandaged, let dry first

Inactive ingredient Purified water

Other information •Keep tightly closed and at controlled room temperature

• does not contain, nor is intended as a substitute for grain or ethyl alcohol

• will produce serious gastric disturbances if taken internally.

For Rubbing & Massaging

Made in India

Imported by: OSTL Inc.

5805 White Oak Ave Encino CA, 91416

WWW.OSTLTRADE.COM

Packaging

IPA 70%

MAXIM 70% ISOPROPYL RUBBING ALCOHOL 
isopropyl alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69950-001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL70 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69950-001-02295 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/17/2016
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A05/17/2016
Labeler - OSTL, INC. (020117798)

Revised: 12/2019
Document Id: 7e8f97bd-bba6-403a-bee4-5955b501ab71
Set id: f6c0cb69-a9d3-407f-8089-3c2930a88165
Version: 2
Effective Time: 20191220
 
OSTL, INC.