Active Ingredient
Isopropyl Alcohol 70%
Alcohol Prep Pad
FDA Label NDC 59194-002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Zhejiang Changdi Medical Co., Ltd. for the product Alcohol Prep Pad (NDC 59194-002). 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, use, warnning, otc - keep out of reach of children, directions, inactive ingredients, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Use
For preparation of skin prior to an injection
Warnning
For External use only.
Flammabel,keep away from fire or flame
Do not use
- with electrocautery procedures,
- in the eyes,
stop use if irritation and redness develop.
Ask a doceor if condition persists for more than 72 hours
Otc - Keep Out Of Reach Of Children
Keep out of reach of children except with adult supervision.
If swallowed,get medical help or contact a Poison Control Center right away.
Directions
wipe injection site vigorously and discard
Other informaiton store at room temperature
Inactive Ingredients
Inactive Ingredients: Water
Package Label.Principal Display Panel
Image Description (03303)
Image Description (626681)
Label (Label)
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