Active Ingredient
Isopropyl Alcohol 70%
Isopropyl Alcohol Spray
FDA Label NDC 67777-011
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Dynarex Corporation for the product Isopropyl Alcohol (NDC 67777-011). 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(s), warnings, do not use, ask a doctor before use if you have, stop use and ask a doctor if, keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
First Aid Antiseptic
Use(S)
• First aid to help prevent infection in minor cuts, scrapes, and burns.
Warnings
For External Use Only
Do Not Use
• Near eyes or mucous membranes • Over large areas of the body • Longer than 1 week unless directed by a doctor • With electrocautery procedures
Ask A Doctor Before Use If You Have
Deep or puncture wounds, animal bites, or serious burns.
Stop Use And Ask A Doctor If
Condition persists for more than 72 hours or get worse.
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.
Directions
• Clean the affected area and spray 1 to 3 times daily • May be covered with a sterile bandage • If bandaged, let dry first
• Children under 12 years of age: Consult a doctor before use
Other Information
• Store at 20°-25°C
• Avoid excessive heat
Inactive Ingredient
Purified Water
Questions?
1-888-Dynarex Monday - Friday, 9AM - 5PM EST
Label 1166
1166_in_master (1166 In Master R240201 5)
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