Drug Facts
Active Ingredient:
Isopropyl Alcohol 70% v/v
Alcohol Prep Pad
FDA Label NDC 81238-0008
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Western First Aid Safety Dba Aramark for the product Alcohol Prep Pad (NDC 81238-0008). 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 drug facts, otc - purpose, indications & usage, warnings, otc - keep out of reach of children, dosage & administration, inactive ingredient, product label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Purpose: Antiseptic
Indications & Usage
Use: for preparation of the skin prior to injection.
Warnings
Warnings:
■ For external use only. ■ Flammable. Keep away
from fire or flame. ■ Do not use: with electrocautery
procedures or in eyes. ■ Stop use: if redness or
irritation develops, if condition continues for more than
72 hours consult a physician.
Otc - Keep Out Of Reach Of Children
■ Keep out of reach from children. If swallowed, get medical attention or
call Poison Control Immediately.
Dosage & Administration
Directions: Apply alcohol as needed to clean intended area. Discard after single use.
Inactive Ingredient
Inactive Ingredients: purified water.
Product Label
NDC 81238-0008-1
aramark
ALCOHOL PREP PAD
MEDIUM
Sterile - Single Use - Latex Free
Saturated with 70% v/v Isopropyl Alcohol
1 Prep Pad [1.2 x 2.6 in. (3 x 6.5 cm)]
Manufactured for Aramark
Lenexa, KS 66219
Made in China
0008-1 (0008 1)
res
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