Active Ingredient
Ethyl alcohol 62%
Sun Bum Hand Sanitizer
FDA Label NDC 69039-615
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Sun Bum Llc for the product Sun Bum Hand Sanitizer (NDC 69039-615). 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 ingredient, purpose, uses, warnings, when using this product, stop use and ask a doctor if, 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
Antiseptic
Uses
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 eye contact, rinse thoroughly with water.
Stop Use And Ask A Doctor If
irritation or rash appears and lasts. Condition persists for more than 72 hours
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
- spray enough product in your palms to thoroughly cover your hands
- rub hands together briskly until dry
- children under 6 years of age should be supervised when using this product
Other Information
- do not store above 104° F/40°C
- may discolor some fabrics or surfaces
Inactive Ingredients
water,fragrance,glycerin,aloe barbadensis leaf juice, cucumis sativus (cucumber) fruit extract, musa sapientum (banana) fruit extract, hedychium coronarium root extract, gardenia taitensis flower extract, cocos nucifera (coconut) oil, sea salt, ethylhexylglycerin
Questions?
1-877-978-6286
Package Labeling:
Bottle5 (Bottle5)
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