Blippi Hand Sanitizer
FDA Label NDC 70108-059
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Ashtel Studios, Inc for the product Blippi Hand Sanitizer (NDC 70108-059). 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 ingredients, purpose, use:, warnings:, • keep out of reach of children., directions:, other information:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredients
Ethyl Alcohol 62% v/v
Purpose
Antiseptic
Use:
To help reduce bacteria and germs on the skin.
Warnings:
For external use only: hands.
Flammable. Keep away from fire or flame.
When using this product:
• Keep out of eyes. • In case of contact with eyes, flush thoroughly with water. • Avoid contact with broken skin. • Do not inhale or ingest.
• Keep Out Of Reach Of Children.
• In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.
Directions:
Put a thumbnail size amount in your palm and rub your hands together briskly until dry. Children under 6 years of age should be supervised when using this product. Not recommended for infants.
Other Information:
• Do not store above 100° F (38°C)
• May discolor some fabrics.
• Harmful to wood finishes & plastics.
Inactive Ingredients:
Water (Aqua), Glycerin, Propylene Glycol, Carbomer, Triethanolamine, Aloe Barbadensis Leaf Extract, Fragrance, Tocopheryl Acetate (Vitamin E), FD&C Blue No. 1
Questions Or Comments?
1-877-274-8358 Toll Free in USA
1-909-434-0911 International
Packaging
Image (Blipi)
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