PHARMA C WIPES 70 ISOPROPYL ALCOHOL- isopropyl alcohol liquid

Pharma C Wipes 70 Isopropyl Alcohol by

Drug Labeling and Warnings

Pharma C Wipes 70 Isopropyl Alcohol 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

Use[s]

first aid to help prevent the risk of infection in: 

minor cuts  scrapes  burns

Warnings

For external use only. FlammableKeep away from heat or flame.

Will produce serious gastric disturbances if taken internally.

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 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.

Caution

- Fumes can be acutely irritating to skin, eyes and the respiratory system. Do not apply to irritated skin or if excessive irritation develops. Avoid getting into the eyes or on mucous membrenes. Avoid getting this product.

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

• does not contain, nor is intended to be a subsititute for ethyl or grain alcohol 
• store at room temperature

Inactive ingredient

purified water

Questions or comments?

1-844-308-8600

Package Labeling:

INGREDIENTS AND APPEARANCE

PHARMA C WIPES 70 ISOPROPYL ALCOHOL 
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55239-327
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	0.7 mL  in 1 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55239-327-00	88 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/01/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	02/01/2022

Labeler - Kleen Test Products Corporation (168165814)