Kndr Sanitizer Gel
FDA Label NDC 78768-004
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Crop Beauty Group Inc. for the product Kndr Sanitizer (NDC 78768-004). 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 drug facts, active ingredient, purpose, use, warnings, when using this product, stop use and ask a doctor if, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Alcohol 62%
Purpose
Antiseptic.
Use
For handwashing to decrease bacteria on the skin.
Warnings
For external use only
Flammable, keep away from fire and flame
When Using This Product
- Avoid the eyes and mucous membranes.
- In the case of eyes or mucous membranes contact,rinse area thoroughly with water.
Stop Use And Ask A Doctor If
- Condition worsens.
- Redness or irritation develops.
- Condition persists for more than 3 days.
Keep Out Of Reach Of Children.
If swallowed,contact a doctor or Poison Control Center immediately.
Directions
Wet hands thoroughly with product and allow to dry without wiping.
Other Information
- Store below 105 °F.
- May discolor some fabrics.
Inactive Ingredients
Water, Aloe Barbadensis Extract, Carbomer, Aminomethyl Propanol, Fragrance.
Package Labeling:
Bottle4 (Bottle4)
* Please review the disclaimer below.
