Alcohol Prep
FDA Label NDC 73161-000

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Handy Care Ltd. Dba Cbd Wipes for the product Alcohol Prep (NDC 73161-000). 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 ingredients, purpose, use, warnings, do not use, stop use, 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

Active Ingredients

Isopropyl Alcohol 70%

Purpose

Antiseptic

Use

For preparation of the skin prior to injection.

Warnings

  • For external use only.
  • Flammable, keep away from fire or flame.

Do Not Use

  • with electrocautery procedures.
  • If in the eyes contact occurs, flush eyes with water.

Stop Use

If irritation and redness develop. If condition continues, consult your health care practitioner.

Keep Out Of Reach Of Children.

If swallowed,get medical help or contact a Poison Control Center right away.

Directions

  • Wipe desired area and discard.

Other Information

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

Inactive Ingredients

purified water

Package Labeling:

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