Walgreen Alcohol Swab
FDA Label NDC 0363-0809

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Walgreens Company for the product Walgreen Alcohol (NDC 0363-0809). 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

Purified water

Package/Label Principal Display Panel

Alcohol Prep Pads

Isopropyl Alcohol 70%

Antiseptic for preparation of the skin prior to injection

200 INDIVIDUAL FOIL PACKETS

STERILE

200 Individual Foil Packets

1.1 IN X 1.33 IN (2.8 cm x 3.4 cm)

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