Alcohol Prep Pad
70% Isoprppyl Alcohol
Alcohol Prep Pad Sponge
FDA Label NDC 69250-661
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Biomed Resource Inc. for the product Alcohol Prep Pad (NDC 69250-661). 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 package label.principal display panel, alcohol prep pad, otc - purpose, otc - keep out of reach of children, otc - do not use, inactive ingredient, dosage & administration, indications & usage, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Antispectic. For preparation of skin prior of injection.
Otc - Keep Out Of Reach Of Children
In case of accidental ingestion, contact your phisician or Poison Control Center right away.
Otc - Do Not Use
Do not use with electrocautery procedures.
Inactive Ingredient
Purified water.
Dosage & Administration
One piece at the time, Discard after use.
Indications & Usage
Wipe injection site vigorously.Discard after use.
Warnings
1. For external use only;
2. Flammable. Keep away from heat or flame;
3. Aviod to contact eyes. Flush throoughly with water in case of contact;
4. Stop use if irritation or redness develop;
5. Do not use with electrocautery procedures;
Keep out of reach of children.
* Please review the disclaimer below.
