Active Ingredient
Ethyl Alcohol 64%
Hand Sanitizer
FDA Label NDC 65692-2073
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Raining Rose for the product Hand Sanitizer (NDC 65692-2073). 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, otc - purpose, indications & usage, warnings, otc - keep out of reach of children, dosage & administration, other safety information, inactive ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Antibacterial
Indications & Usage
Uses - Hand Sanitizer to help reduce bacteria on the skin. - Recommended for repeated use.
Warnings
- For external use only. Flammable, keep away from fire or Flame. - Do not use in eyes. In case of eye contact, flush throroughly with water and seek medical attention. -Stop use and ask doctor if irritation and redness develop and 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.
Dosage & Administration
Directions
- Dispense an adequate amount in your palm to cover all surfaces of hands completely
- Rub hands together until dry
- Does not require rinsing
Other Safety Information
- Do not store above 105 °F
- May discolor some fabrics
Inactive Ingredient
Water, Glycerin, Carbomer, Diisopropylamine, Fragrance
* Please review the disclaimer below.
