Active Ingredient
Benzalkonium Chloride 0.1% Antimicrobial
Sweet Skin Hand Sanitizer
FDA Label NDC 80958-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Sweet Skin Etc. Llc for the product Sweet Skin Hand Sanitizer (NDC 80958-001). 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, otc - 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
Antimicrobial
Uses
- For hand sanitizing to decrease bacteria on skin
- Recommended for repeated use
Warnings
For external use only. Do not use if you are allergic to any of these ingredients
When Using This Product
avoid contact with eyes. In case of contact, flush eyes with water.
Stop Use And Ask A Doctor
if irritation of redness develops, or if condition proceeds for more than 72 hours.
Otc - Keep Out Of Reach Of Children
Children under two consult a doctor before usage.
Directions
Adults and children 2 years and over: apply to hands; allow to dry without wiping.
Children under two consult a doctor before usage.
Inactive Ingredients
Aloe 0.1%, glycerol polyether and water
Package Label - Principal Display Panel
3.785 L NDC: 80958-019-01
ALCOHOL FREE
SWEET
SKIN etc.
HAND SANITIZER
Enriched with ALOE
1 GALLON
Pdp (80958 001 01)
* Please review the disclaimer below.
