The Nordic Shield Sanitizer Wipes
FDA Label NDC 79232-900
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by The Nordic Shield Aps for the product The Nordic Shield Sanitizer Wipes (NDC 79232-900). 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, purpose, uses, warnings, otc - keep out of reach of children, directions, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Alcohol 75% v/v
Purpose
Antiseptic
Uses
For sanitizing to help reduce bacteria on the skin.
Warnings
For external use only. Flammable. Keep away from heat or flame.
Do not use
• in or near the eyes.
• on open skin wounds or burns
Otc - Keep Out Of Reach Of Children
Keep out of reach of children unless under adult supervision. If swallowed, get medical help or contact a poison control center right away.
Directions
• Open lid, gently pull back resealable label, remove and use wipe as required.
• Reseal back after use to avoid evaporation of alcohol.
Other Information
This product is insoluble in water. Dispose of used wipe in trash, do not flush into toilet. This product may discolor certain fabrics or surfaces.
Inactive Ingredients
Water (Aqua)
Packaging
Image (7923290050)
* Please review the disclaimer below.
