Clorox Hand Sanitizer Gel
FDA Label NDC 69540-0025
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Brand Buzz Llc for the product Clorox Hand Sanitizer (NDC 69540-0025). 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 drug facts, active ingredient, purpose, use, warnings, when using this product, discontinue use, 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
Active Ingredient
Ethyl Alcohol 71% v/v
Purpose
Antiseptic
Use
Hand sanitizer to help reduce bacteria on the skin. Recommended for repeated use.
Warnings
For external use only. Flammable. Keep away from fire or flame.
When Using This Product
do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.
Discontinue Use
if irritation and redness develop. If condition persists for more than 72 hours consult a physician.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away
Directions
- Squeeze gel into your palm and briskly rub hands together until dry.
- Children under 6 years of age should be supervised when in use.
Other Information
- Store between 15 and 30C (59 and 86F).
- Avoid freezing and excessive heat above 40C (104F).
Inactive Ingredients
Aloe Barbadensis Leaf Extract, Carbomer, Glycerin, Tocopheryl Acetate (Vitamin E), Triethanolamine, Water (Aqua).
Package Labeling:2Ml
Label (Label)
Box (Box)
Package Labeling:500Ml
Label2 (Label2)
Package Labeling:1000Ml
Label4 (Label4)
Package Labeling:1000Ml Refill
Bottle (Bottle)
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