Active Ingredients
Isopropyl Alcohol 70%
Alcohol Wipe
FDA Label NDC 50428-0030
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Dorel Juvenile Group for the product Alcohol Wipe (NDC 50428-0030). 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, 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
Purpose
Topical Antimicrobial use
Use
To prep skin prior to antimicrobial use.
Warnings
- For external use only
- Flammable, keep away from fire or flame
Do Not Use
- With electrocautery procedures
- In the eyes
Stop Use
if irritation or redness develop. If the condition persists for more than 72 hours, consult a doctor.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Clean and discard.
Other Information
Store at room temperature 15°C - 30°C (59°F - 86°F)
Inactive Ingredients
purified water
Package/Label Principal Display Panel
1st™ Alcohol Wipe
70% Isopropyl Alcohol
EXTERNAL USE ONLY
For Home Use only
© 2012 Dorel Juv. Grp., Columbus, IN
1-877-657-9545 Made in CHINA
Model No. AL-01 NDC# 50428-0030
Package Label (285f23e4 84e6 4930 Ba12 C7626713d2cb 01)
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