Otc - Active Ingredient
Ethyl Alcohol 70.0% v/v
Hand Sanitizer 1.8 Oz Antiseptic Liquid
FDA Label NDC 57337-107
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Rejoice International Corp. for the product Hand Sanitizer 1.8 Oz Antiseptic (NDC 57337-107). 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 otc - active ingredient, otc - purpose, indications & usage, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Anitseptic
Indications & Usage
- to decrease bacteria on the skin that could cause disease
- recommended for repeated use
Warnings
For external use only: hands
Flammable, keep away from fire or flame
Otc - When Using
- keep out eyes. In case of contact with eyes, flush thoroughly with water
- avoid contact with broken skin
- do not inhale or ingest
Otc - Stop Use
Stop use and ask a doctor if irritation and redness develop and persist 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.
Dosage & Administration
- spray hand thoroughly with product and allow to dry without wiping
- for children under 6, use only under adult supervision
- not recommended for infants
Other Safety Information
- store at room temperature
- may discolor certain fabrics
- harmful to wood finished and plastics
Inactive Ingredient
water, glycerin, tocopheryl acetate, aloe barbadensis leaf juice, fragrance.
* Please review the disclaimer below.
