Active Ingredient
Isopropyl Alcohol 70%
Alcohol Prep
FDA Label NDC 76161-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Kyj Medical Products Co.,ltd. for the product Alcohol Prep (NDC 76161-001). 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, directions, inactive ingredients, otc - keep out of reach of children, 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
Use for preparation of the skin prior to an injection
Warnning
For External use only.
Flammable,keep away from fire or flame.
Do not use with electrocautery procedures in 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 in case of accidental ingestion,seek professional assistance or consult a Poison Control Center immediately.
Directions
Apply alcohol as needed to clean intended area. Discard after single use.
Inactive Ingredients
Inactive Ingredients: Purified Water
Otc - Keep Out Of Reach Of Children
Keep out of reach of children in case of accidental ingestion,seek professional assistance or consult a Poison Control Center immediately.
Package Label.Principal Display Panel
Kyj (Kyj)
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