Use(S)
To help reduce bacteria on the skin. For use when soap and water are not available.
Hand Sanitizer
FDA Label NDC 75023-003
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 Wave Wellness, Llc for the product Hand Sanitizer (NDC 75023-003). 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 use(s), warnings, do not use, when using this product, stop use and ask a doctor if, 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
Warnings
For external use only.
Flammable. Keep away from heat or flame.
Do Not Use
- on children less than 2 months of age
- on open skin wounds
- around eyes
- in ears and mouth
When Using This Product
keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
- avoid contact with broken skin
- do not inhale or ingest
Stop Use And Ask A Doctor If
irritation or rash occurs.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
- Place enough product on hands to cover all surfaces. Rub hands together until dry.
- Supervise children under 6 years of age when using this product to avoid swallowing.
Other Information
- Store between 15-30C (59-86F)
- Avoid freezing or excessive heat above 40C (104F).
Inactive Ingredients
Aloe Barbadensis (leaf) Extract, Fragrance, Glycerin, Purified Water
Manufactured By:
Sun Wave Wellness, LLC
1419 Chaffee Drive #101
Titusville, FL 32780-7933
Drug Facts
Active Ingredient(S)
Alcohol 70% v/v
Purpose
Antiseptic
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