Active Ingredient
Alcohol 69% v/v
Ultra Defense Sani Smart Moisturizing And Sanitizer
FDA Label NDC 74177-955
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by K7 Design Group Inc. for the product Ultra Defense Sani Smart Moisturizing And Sanitizer (NDC 74177-955). 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, uses, warnings, when using this product, stop use and ask a doctor if, keep out of reach of children., directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Uses
- to decrease bacteria on the skin that could cause disease
- recommended for repeated use
Warnings
For external use only
Flammable, keep away from fire or flame.
When Using This Product
- keep out of eyes. In case of contact with eyes, flush thoroughly with water
- avoid contact with broken skin
- do not inhale or ingest
Stop Use And Ask A Doctor If
- irritation and redness develop and persist for more than 72 hours
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away
Directions
- Spray directly on hands and rub in thoroughly
- For children under 6, use adult supervision
- Not recommended for infants
Other Information
- Store between 15-30 C (59-86F)
- Avoid freezing and excessive heat above 40C (104F)
Inactive Ingredients
Water, Aloe Barbadensis Leaf Extract, Tocopheryl Acetate, Fragrance, Denatonium Benzoate.
Company Information
MANUFACTURED FOR & DISTRIBUTED BY K7 DESIGN GROUP LLC. 2433 KNAPP STREET, BROOKLYN, NY 11235
ORIGIN: CHINA
Product Packaging
Kit1 (Kit1)
* Please review the disclaimer below.
