Alcohol Prep Pad
FDA Label NDC 69139-001

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Yiwu Haoding Medical Co.,ltd for the product Alcohol Prep Pad (NDC 69139-001). 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, warnning, otc - keep out of reach of children, directions, inactive ingredients, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Isopropyl Alcohol 70%

Purpose

Antiseptic

Use

For preparation of skin prior to an injection 

Warnning

For External use only.

Flammabel,keep away from fire or flame

Do not use

  • with electrocautery procedures or in the eyes,

    • stop use if irritation and redness develop. if condition persists for more than 72 hours consult a physician.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children

if ingested,do not induce vomiting,get medical help or contact a poison Control Center right immediately.

Directions

Apply alcohol as needed to clean intended area ,discard after single use.

Inactive Ingredients

purified water

Package Label.Principal Display Panel

Label (Label)

Label (Label)

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