Active Ingredient
Ethyl Alcohol 75% v/v
Carecom Hand Sanitizer
FDA Label NDC 76626-004
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Mcrl Overseas Printing Inc for the product Carecom Hand Sanitizer (NDC 76626-004). 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, use, warnings, otc - keep out of reach of children, directions, inactive ingredients, package label - principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Sanitizer
Use
- to decrease bacterias on the skin that could cause diseases.
- recommended for repeated use
Warnings
For external use only-hands. Use only as directed. Excessive use or prolonged exposure may cause irritation to skin. Discontinue use if rash, redness or itching appears. Flammable. Keep away from heat or flame.
When using this product
- keep out of eyes. In case of contact with eyes, immediately flush with water and call a doctor.
- avoid contact with broken skin.
Stop use and ask a doctor if irritation or redness develops.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. In case of accidental ingestion seek professional assistance or contact a poison control center immedietly.
Directions
Put a thumb size amount in your palm and rub hands together briskly until dry.
Other information:
- do not store in temperature over 118F.
- children under the 6 years of age should be supervised while using this product.
- may discolor certain fabrics.
Inactive Ingredients
Water, glycerin, propylene Glycol, carbomer, sodium hydroxide
Package Label - Principal Display Panel
Label
* Please review the disclaimer below.
