Active Ingredients
Ethyl Alcohol 62% V/V
Solar Flare Sunlit Holiday Hand Sanitizers Spray
FDA Label NDC 76891-172
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Scent Theory Products Llc for the product Solar Flare Sunlit Holiday Hand Sanitizers (NDC 76891-172). 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 ingredients, purpose, uses, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antibacterial
Uses
For handwashing to decrease bacteria on the skin.
Warnings
For external use only: hands
Flammable, keep away from fire or flame.
Otc - When Using
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.
Otc - Stop Use
Stop 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 right away.
Directions
Spray hands with product and allow to dry without wiping
For children under 6, use only under adult supervision
Not recommended for infants
Other Information
Do not store above 105°F
may discolor some fabrics
harmful to wood finishes and plastics
Inactive Ingredients
Alcohol Denat., Water (Aqua), Fragrance (Parfum), Glycerin, Aloe Barbadensis Leaf Water. May Contain: Blue 1, Yellow 5, Red 40, Red 33
Package Label.Principal Display Panel
Solarflare_limitededition_handsani_box (Solarflare Limitededition Handsani Box)
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