ISOPROPYL ALCOHOL- isopropyl alcohol liquid 
Medical Chemical Corporation

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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ISOPROPYL ALCOHOL

Antiseptic

Directions: Apply to affected area for first-aid treatment of minor cuts and abrasions.  In case of deep or puncture wounds consult a physician.  Discontinue use and get medical aid if redness, irritation or infection develops.  Apply liberally for rubbing.

Active ingredient:  Isopropyl alcohol, 70%

Warnings:  For external use only.  Avoid contact with eyes or mucous membranes.  Ingestion will result in gastrointestinal distress, unconsciousness and death.  Keep out of reach of children.  In case of ingestion contact a poison control center immediately.

Flammable: Avoid sources of ignition.  Do not use around open flames.

Warnings:  For external use only.  Avoid contact with eyes or mucous membranes.  Ingestion will result in gastrointestinal distress, unconsciousness and death.  Keep out of reach of children.  In case of ingestion contact a poison control center immediately.

Inactive Ingredients: Water

Directions:  Apply to affected area for first-aid treatment of minor cuts and abrasions.  In case of deep or puncture wounds consult a physician.  Discontinue use and get medical aid if redness, irritation or infection develops.  Apply liberally for rubbing.

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ISOPROPYL ALCOHOL 
isopropyl alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:12745-105
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL70.14 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:12745-105-01946 mL in 1 BOTTLE, PLASTIC; Type 1: Convenience Kit of Co-Package06/15/1954
2NDC:12745-105-033785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/15/1954
3NDC:12745-105-043785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/15/1954
4NDC:12745-105-0518927 mL in 1 CONTAINER; Type 0: Not a Combination Product06/15/1954
5NDC:12745-105-0618927 mL in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK; Type 0: Not a Combination Product06/15/1954
6NDC:12745-105-07208198 mL in 1 DRUM; Type 0: Not a Combination Product06/15/1954
7NDC:12745-105-08473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/15/1954
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34406/15/1954
Labeler - Medical Chemical Corporation (008496861)
Establishment
NameAddressID/FEIBusiness Operations
Medical Chemical Corporation008496861manufacture(12745-105)

Revised: 1/2022
Document Id: d5d0dbef-b098-542b-e053-2a95a90ad350
Set id: a04239d8-0fa9-4c00-aa81-d7a1242bc931
Version: 18
Effective Time: 20220117
 
Medical Chemical Corporation