Drug Facts
Active Ingredient[s]
Ethyl Alcohol 65%
Swedish Dream Sea Aster Hand Sanitizer
FDA Label NDC 79655-608
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 Aster Hand Sanitizer (NDC 79655-608). 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, purpose, uses, warnings, when using this product, stop use and ask a doctor, 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
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.
Stop Use And Ask A Doctor
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
Apply on hands, rub until dry.
Other Information:
Store between 15-30C (59-86F) • Avoid freezing and excess heat above 40C (104F).
Inactive Ingredients
Deionized water, Glycerine, Fragrance Oil
Seaweed Hand Sanitizer & Sea Aster Hand Sanitizer Label
Sea Aster Hand Sanitizer (Sea Aster Sanitizer Wc4 Outlines)
Seaweed Hand Sanitizer (Seaweed Sanitizer Wc4 Outlines)
* Please review the disclaimer below.
