Active Ingredient
Ethyl Alcohol 70% v/v
Hand Sanitizer
FDA Label NDC 70897-012
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Davemed Healthcare Co., Ltd for the product Hand Sanitizer (NDC 70897-012). 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, uses, warning:, when using this product:, stop use and ask a doctor:, keep out of children:, directions:, ingredients:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Uses
To decrease bacteria on the skin that could cause disease.
Recommended for repeated use.
Warning:
Flammable.
Keep away from fire or flame.
For external use of onlyh.
When Using This Product:
avoid contact with eyes in case of eye contact immediately flush eyes with water, call a doctor avoid contact with broken skin.
Stop Use And Ask A Doctor:
Discontinue use if irritation or redness develos, If condition persists from more than 72 hours, consult a doctor
Keep Out Of Children:
Children should only use this product under adult supervision
Directions:
- Place enough product in your palm to thoroughly spread on both hands and rub into the skin undil dry Recommended for repeated use.
Ingredients:
Water, Alcohol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Peg-40, Hydrogenated Castor Oil, Parfum, Triethanolamine
Otc - Purpose
Antiseptic
Other Safety Information
Do not drink. Not edible. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately
- Store between 15-30C
- Avoid freezing and excessive heat above 40C (104F)
* Please review the disclaimer below.
