Alcohol
FDA Label NDC 71622-004

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Mcl Enterprises for the product Alcohol (NDC 71622-004). 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:, 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 Ingredient

Isopropyl Alcohol, 70% v/v

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:

  • longer than 1 week 
  • in the eyes

Stop Use:

  • if irritation and redness develop. If condition persists consult a doctor.

Keep Out Of Reach Of Children.

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

Directions:

Apply topically to cleanse the intended area and discard after single use.

Inactive Ingredient:

Purified Water

Package Labeling:

Label4 (Label4)

Label4 (Label4)

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