Active Ingredient
Alcohol 75%
Apollo Instant Hand Sanitizer
FDA Label NDC 78303-002
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. for the product Apollo Instant Hand Sanitizer (NDC 78303-002). 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, otc - when using, otc - stop use, otc - 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:
Hand sanitizer to help decrease bacterial 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.
Otc - When Using
When using this product,
Avoid contact with eyes. In case of contact flush eyes with water.
Otc - Stop Use
Stop use and ask a doctor
If redness or irritation develop and persist for more than 72 hours
Otc - Keep Out Of Reach Of Children
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℉（43℃）
May discolor certain fabrics or surfaces.
Inactive Ingredients
Water, Glycerin, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Fragrance, Aminomethyl Propanol, Propylene Glycol, Tocopherol, Disodium EDTA, Aloe Barbadensis Leaf Juice Power, Lactic Acid, Citric Acid.
Pdp
3785ml NDC: 74658-009-01
* Please review the disclaimer below.
