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Distributed by Obagi Cosmeceuticals LLC,
Long Beach, CA 90806
Obagi Medical Hand Sanitizer
FDA Label NDC 62032-003
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Obagi Cosmeceuticals Llc for the product Obagi Medical Hand Sanitizer (NDC 62032-003). 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 other, active ingredients, purpose, use, warnings, otc - when using, otc - keep out of reach of children, otc - stop use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredients
Ethyl Alcohol 65%
Purpose
Antiseptic
Use
helps decrease bacteria on the hands
Warnings
Flammable. Keep away from fire or flame.
For external use only
Otc - When Using
When using this product, avoid contact with eyes. In case of contact, rinse eyes thoroughly with water immediately
Otc - Keep Out Of Reach Of Children
Keep out of reach of children except under adult supervision. If swallowed, get medical help or contact a poison control center right away.
Otc - Stop Use
If irritation develops, discontinue use and consult a doctor.
Directions
- Dispense a small amount on palms. Rub lightly until dry. Do not rinse.
Other Information
- Store below 105°F (40°C)
Inactive Ingredients
Water (Aqua), Glycerin, Isopropyl Alcohol, Butylene Glycol, Carbomer, Aminomethyl Propanol, Isopropyl Myristate, Tocopheryl Acetate
Questions Or Comments?
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Principal Display Panel - 59 Ml Bottle Label
OBAGI™
MEDICAL
HAND
SANITIZER
2 FL. OZ. (59 mL)
Principal Display Panel (59 mL Bottle Label)
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