FDA Label for Clorox Hand Sanitizer
View Indications, Usage & Precautions
Clorox Hand Sanitizer Product Label
The following document was submitted to the FDA by the labeler of this product The Clorox Company. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Active Ingredient
Alcohol 71% v/v
Purpose
Antiseptic
Use
Hand sanitizer to help decrease bacteria on skin that can potentially cause disease.
Warnings
Flammable. Keep away from fire or flame.
For external use only.
Otc - Do Not Use
Do not use in the eyes.
Otc - Stop Use
Discontinue use and ask a doctor if
- irritation and redness develop.
- condition persists for more than 72 hours.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a poison control center immediately.
Directions
- Spray on clean, dry hands and nails
- Wet hands thoroughly with product
- Rub hands together for no less than 15 seconds, paying particular attention to interdigital spaces, fingernails and cuticles
- Allow to dry without wiping
- Rub hands together briskly until dry
Other Information
- Store in a cool, dry place below 104 deg F (40 C)
Inactive Ingredients
Water, Isopropyl Alcohol, Glycerin, Glyceryl Laurate
Questions Or Comments?
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Package Label.Principal Display Panel
Clorox
Commercial
Solutions
CLOROX
BLEACH-FREE
Hand Sanitizer
Kills greater than
99.999%* of
germs on contact
Contains hand moisturizers
Alcohol-based
*of FDA organisms in the TFM for
Topical Antimicrobial Drug
Products
16.9 FL OZ I 500 mL
* Please review the disclaimer below.