Active Ingredient
Isopropyl Alcohol, 70% v/v
Alcohol Prep Pad
FDA Label NDC 68345-721
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Pss World Medical, Inc. for the product Alcohol Prep Pad (NDC 68345-721). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient, purpose, use, warnings, do not use, stop use and ask a doctor if, keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Use
For preparation of skin prior to injection
Warnings
For external use only.
Flammable, keep away from fire or flame.
Do Not Use
Do not use:
- with electrocautery procedures
- in the eyes.
Stop Use And Ask A Doctor If
irritation or redness develop. If the condition persists for more than 72 hours, consult a doctor.
Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Contents sterile until opened.
Wipe injection site vigorously and discard.
Inactive Ingredients
Purified water
Questions
Questions or Comments about Select Medical Products? 800-777-4908
Manufactured for PSS World Medical, Inc.
4345 Southpoint Blvd., Jacksonville, FL 32216
Made in China
Principal Display Panel
68345-721-01
521 ALCOHOL PREP PAD
2 Ply Medium Sterile
For preparation of the skin prior to injection
Single use only.
Sterile unless package is opened or damaged.
68345-720-01
527 ALCOHOL PREP PAD
2 Ply Lightweight Medium Sterile
For preparation of the skin prior to injection
Single use only.
Sterile unless package is opened or damaged.
* Please review the disclaimer below.
