Swirling Lollipop
FDA Label NDC 50157-114
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Brands International Corp for the product Swirling Lollipop (NDC 50157-114). 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 package label, otc - active ingredient, otc - purpose, indications & usage, warnings, otc - keep out of reach of children, otc - when using, otc - ask doctor, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Active Ingredient
ACTIVE INGREDIENTS: Ethyl Alcohol 62%
Otc - Purpose
Antiseptic
Indications & Usage
Use
- To decrease bacteria on the skin and clean hands.
- Recommended for repeated use.
Warnings
Warnings
For external use only.
Flammable, keep away from fire or flame.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If accidentally swallowed get medical help or contact a Poison Control Center right away.
Otc - When Using
Do not get into eyes. If contact occurs, rinse thoroughly with water.
Otc - Ask Doctor
Discontinue use if irritation or redness develop. If irritation persists for more than 72 hours, consult a doctor.
Dosage & Administration
Directions
- apply to hands until thoroughly wet
- rub vigorously until dry
- supervise children in the use of this product
Other Safety Information
- may discolor certain fabrics or surfaces
- do not store above 110°F (43°C)
Inactive Ingredient
Water, Isopropyl Alcohol, Glycerin, Carbomer, Aminomethyl Propanol, Fragrance, Propylene Glycol, Isopropyl Myristate, Aloe Barbadensis Leaf Juice, Tocopheryl (Vitamin E) Acetate, Sunflower (Helianthus Annuus) Seed Extract, Yellow 5 (Cl 19140), Blue 1 (Cl 42090)
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