Alcohol Swab
FDA Label NDC 41163-816

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Supervalu, Inc. for the product Alcohol (NDC 41163-816). 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, uses, 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

Active Ingredient

Isopropyl alcohol, 70% v/v

Purpose

Antiseptic

Uses

  • 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
  • in the eyes

Stop Use And Ask A Doctor If

  • irritation and redness develop
  • condition persists for more than 72 hours

Keep Out Of Reach Of Children.

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

Directions

Wipe injection site vigorously and discard

Other Information

Protect from freezing. Avoid excessive heat.

Inactive Ingredients

water

Package/Label Principal Display Panel

equaline

compare to B-D Alcohol Swabs active ingredient*

NDC 41163-816-30

sterile

alcohol prep swabs

  • saturated with isopropyl alcohol 70%
  • antiseptic for preparation of the skin prior to injection
  • safe and easy to use

    • 100 individual packets

* Please review the disclaimer below.