Nordland Hand Sanitizer
FDA Label NDC 90029-000
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Nordland Development, S. De R.l. De C.v. for the product Nordland Hand Sanitizer (NDC 90029-000). 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, do not use, when using this product, stop use and ask a doctor, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient(S)
Ethyl Alcohol 70% v/v
Purpose
Antiseptic
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. Flammable. Keep away from heat or flame.
Do Not Use
in children less than 2 months of age
- on open skin wounds
When Using This Product
keep out of eyes, ears and mouth. In case of contact with eyes, rinse eye thoroughly with water.
Stop Use And Ask A Doctor
if irritation or rash occurs. These may be signs of a serious condition.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Place enough product on hands to cover
- all surfaces. Rub hand together until dry. Supervise children under 6 years of age
- when using this product to avoid swallowing.
Inactive Ingredients
Glycerin, distilled water, triethanolamine, carbomer and fragrance
Package Labeling:
Bottle2 (Bottle2)
* Please review the disclaimer below.
