Rainbow Hand Sanitizer Yellow
FDA Label NDC 75063-0010
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Belleson Inc for the product Rainbow Hand Sanitizer Yellow (NDC 75063-0010). 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, uses, warnings, directions, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Ethyl Alcohol 68% v/v
Purpose
Antiseptic
Uses
Hand sanitizer to help reduce bacteria that potentially can cause
disease. For use when soap and water are not available.
Warnings For external use only. Flammable. Keep away from heat or flame
Warnings
Do not use
• in children less than 2 months of age
• on open skin wounds
When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
• Place enough product on hands to cover all surfaces. Rub hands together until dry.
• Supervise children under 6 years of age when using this product to avoid swallowing.
Other Information
Store between 15-30C (59-86F) • Avoid freezing and excessive
heat above 40C (104F)
Inactive Ingredients
Aqua, Glycerin, Aloe Vera Leaf, Mugwort Extract, Calendula Officinalis Flower,Camellia Sinensis Leaf Extract, Mulberry Root Extract, Licorice Extract,Rosmarinus Officinalis (Rosemㅍvary) Leaf Oil, Polysorbate 20, Fragrance, FD&C Yellow No. 5
Product Label
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