Active Ingredient
Ethyl Alcohol 62%
Hand Sanitizer
FDA Label NDC 73711-103
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Spinster Sisters, Inc. for the product Hand Sanitizer (NDC 73711-103). 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, do not use, 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
Reduces bacteria on the skin
Warnings
- For external use only.
- Flammable. Keep away from fire and sparks. Do not store above 104°F/40°C.
Do Not Use
near eyes. In case of contact with eyes, rinse with water.
Stop Use And Ask A Doctor
if skin irritation develops.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center immediately.
Directions
Rub dime-sized amount on hands. Supervise children under 6.
Inactive Ingredients
Aloe Vera Gel [Aloe Barbadensis, Citric Acid, Sodium Benzoate, Potassium Sorbate, Sodium Sulfite], Mentha Piperita (Peppermint) Oil, Melaleuca Alternifolia (Tea Tree) Oil, and Glycerin
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