Alcohol Prep Pads
FDA Label NDC 11673-141
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Target Corporation for the product Alcohol Prep Pads (NDC 11673-141). 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, uses, warnings, do not use, otc - ask doctor/pharmacist, otc - when using, stop use and ask a doctor, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Topical Anesthetic
Antiseptic
Uses
- For preparation of the skin prior to injection
- For temporary relief of pain and itching associated with minor burns, sunburn, minor skin irritations, or insect bites
Warnings
For external use only.
Flammable, keep away from fire or flame.
Do Not Use
- in the eyes
- with electrocautery procedures
Otc - Ask Doctor/Pharmacist
Otc - When Using
Stop Use And Ask A Doctor
- if irritation and redness develop
- if symptoms persist for more than 72 hours or symptoms clear up and occur within a few days.
Ask A Doctor Or Pharmacist
if you are pregnant or nursing a baby.
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Other
Other Information
- Store at room temperature: 15° - 30° C (59° - 86° F)
- Do not use to clean and disinfect medical devices or on hard surfaces
Inactive Ingredients
Questions?
Call 1-800-910-6874
Package Information
NDC 11673-141-31
alcohol prep pads
with benzocaine
for preparation of the skin
prior to injection
up and up
80 count
80 INDIVIDUALLY WRAPPED PADS
245 10 0155 ID120478
Distributed by Target Corporation
Minneapolis, MN 55403
Made in U.S.A
©2010 Target Brands, Inc.
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