THE PHARMA-C COMPANY 70 ISOPROPYL ALCOHOL WIPES- isopropyl alcohol cloth

The Pharma-C Company 70 Isopropyl Alcohol Wipes by

Drug Labeling and Warnings

The Pharma-C Company 70 Isopropyl Alcohol Wipes by is a Otc medication manufactured, distributed, or labeled by Kleen Test Products Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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.

Flammablekeep away from fire or flame, heat, spark, electrical 

Ask a doctor before use if you have

deep or puncture wounds  animal bites  serious burns

When using this product

do not get in 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 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 product on the affected area of the body 1 to 3 times a day  may be covered with a sterile bandage  if bandaged, let dry first

Other information

do not apply internally  keep canister tightly closed and stored at room temperature  hold away from face when opening

Inactive ingredients

purified water

Questions or comments?

1-844-308-8600

Package Labeling: (40 Count)

Package Labeling: (175 Count)

INGREDIENTS AND APPEARANCE

THE PHARMA-C COMPANY 70 ISOPROPYL ALCOHOL WIPES 
isopropyl alcohol cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55239-362
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55239-362-00	40 in 1 CANISTER	03/01/2019
1		4.5 mL in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
2	NDC: 55239-362-01	175 in 1 CANISTER	10/01/2022
2		5.2 mL in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	03/01/2019

Labeler - Kleen Test Products Corporation (168165814)

Registrant - Kleen Test Products Corporation (168165814)