Active Ingredient
Ethyl Alcohol 65%
Swedish Dream Sea Salt Hand Sanitizer
FDA Label NDC 79655-606
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Kala Corporation for the product Swedish Dream Sea Salt Hand Sanitizer (NDC 79655-606). 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, keep out of reach of children, directions:, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Uses
Sanitizer to help reduce bacteria on skin. For use when soap and water not available.
Warnings
For external use only. Keep away from heat or flame.
When Using This Product
Keep out of eyes. In case of contact, flush thoroughly with water.
Keep Out Of Reach Of Children
If swallowed get medical help or contact a poison control center right away.
Directions:
Apply on hands and rub until dry.
Other Information
Store between 15-30C(59-86F) - Avoid freezing and excess heat over 40C(104F)
Inactive Ingredients
Deionized Water, Glycerine, Sea Salt Essence (Fragrance Oil)
Sea Salt Hand Sanitizer Label
Sea Salt Hand Sanitizer (Made in the Ocean State)
* Please review the disclaimer below.
