Purpose
Alcohol 80% v/v ……… Antiseptic
Hand Sanitizer
FDA Label NDC 78816-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Blackland Distillery for the product Hand Sanitizer (NDC 78816-001). 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 purpose, uses, warning, do not use, 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
Uses
Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.
Warning
For external use only – hands
Flammable
Keep away from fire and flame
Do Not Use
- on 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 thoroughly with water.
Stop Use And Ask A Doctor If
irritation or rash occurs. These may be a sign of a serious condition.
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right way.
Directions
Place enough product on hands to cover all surfaces. Rub hands until dry.
Supervise children under 6 years of age who are using this product to avoid swallowing.
Other Information
Store between 15 ° - 30 ° C (59° - 86°F)
Avoid freezing and excessive heat above 40°C (104°F)
Inactive Ingredients
Aloe, Fragrance, Glycerin, Hydrogen Peroxide, Reverse Osmosis Water
Principal Display Panel
Hand Sanitizer
Juniper scent
8 fl oz (237 ml)
Principal Display Panelhand Sanitizerjuniper Scent8 Fl Oz (237 mL) (Hand Sanitizer 01)
* Please review the disclaimer below.
