Sanitizer Station Hand Sanitizer Foam
FDA Label NDC 82062-201
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Pharmore Group Llc Dba Sanitizer Station for the product Sanitizer Station Hand Sanitizer Foam (NDC 82062-201). 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[s], purpose, use[s], warnings, otc - keep out of reach of children, directions, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient[S]
Benzalkonium Chloride 0.13%
Purpose
Antimicrobial
Use[S]
Hand sanitizer to help reduce bacteria that potentially can cause disease.
For use when soap and water are not available.
Warnings
For external use only.
Do not use
• in children less than 2 months of age
• on open skin wounds
When using this product avoid contact with eyes.
In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask doctor if irritation or redness develops, or if condition persists for more than 72 hours.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
- Pump a small amount of foam into palm of hand.
- Rub thoroughly over all surfaces of both hands.
- Continue to rub hands until dry.
Inactive Ingredients
deionized water, glycerin, aloe barbadensis leaf juice, lauramine oxide, dimethyltetradecylamine oxide, fragrance, DMDM hydantoin (preservative).
Packaging
Foam (82062 201 50 3)
* Please review the disclaimer below.
