THESIS PHARMACY ALCOHOL PREP PAD- isopropyl alcohol cloth

Drug Labeling and Warnings

Drug Details [pdf]

Drug Facts

Active ingredient

Isopropyl Alcohol, 70% v/v

Purpose

Antiseptic

Use

For preparation of skin prior to injection.

Warnings

For external use only. Flammable, Keep away from fire of flame. Do not use  with electrocautery procedures in the eyes  on mucous membranes on irritated skin. Stop use and ask a doctor if  irritation or redness develops.

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

Directions

Wipe injection site vigorously and discard.

Other information

Store at room temperature 15 - 30°C(59 - 86°F)

Inactive ingredients:

Purified Water

SPL UNCLASSIFIED SECTION

Precision. Trust. Compassion.

Medium
60mm×30mm

Apply topically as needed to cleanse intended area.
Apply the product to the skin, take the injection or puncture site as the center, slowly rotate from the inside to the
outside, and gradually apply the product for two times, the disinfection area should be more than 5cmx5cm, and the
action time should be 1min.
Use for preparation of skin prior to injection, apply the product to the skin, take the injection or puncture site as the
center, slowly rotate from the inside to the outside, and gradually apply the product for two times, the disinfection area
should be more than 5cmx5cm, and the action time should be 1min. Please clean before disinfection

Single use only

STERILE R

Manufactured in China for:
Carelife USA
Alpharetta, GA
www.carelife-usa.com

CAUTION:Sterility of contents guaranteed in unopened, undamaged package.

LATEX free

Made in China

Packaging

INGREDIENTS AND APPEARANCE

THESIS PHARMACY ALCOHOL PREP PAD 
isopropyl alcohol cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71749-001
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: 71749-001-01	100 in 1 BOX	03/30/2026
1		1 in 1 POUCH
1		0.4 mL in 1 PATCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	03/30/2026

Labeler - Carelife (USA) Inc. (065756949)