Apollo Instant Hand Sanitizer
FDA Label NDC 78303-000
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Sbu Group L.p. Dba Apollo Distributors for the product Apollo Instant Hand Sanitizer (NDC 78303-000). 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, active ingredient, purpose, uses, warnings, when using this product,, stop use and ask a doctor, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Ethyl Alcohol 75% v/v
Purpose
Antiseptic
Uses
- Hand sanitizer to help decrease bactrerial on the skin, when water, soap & towel are not available.
- Recommended for repeated use.
Warnings
For external use only. Flammable. Keep away from fire or flame.
Do not apply around eyes. Do not use in ears & mouth.
When Using This Product,
avoid contact with eyes. In case of contact flush eyes with water.
Stop Use And Ask A Doctor
if redness or irritation develop and persists for more than 72 hours.
Keep Out Of Reach Of Children.
Children must be supervised in use of this product.
Directions
- Place enough product into your palms and thoroughly spread on both hands.
- Rub into skin until dry.
Other Information
- Store below 110 °F (43 °C).
- May discolor certain fabrics or surfaces.
Inactive Ingredients
Carbomer, Triethanolamine, Glycerin, Water.
Package Labeling :500Ml
Label5 (Label5)
Package Labeling :237Ml
Label4 (Label4)
Package Labeling :60Ml
Label2 (Label2)
Package Labeling :120Ml
Label3 (Label3)
Package Labeling :5000Ml
Label (Label)
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