Active Ingredient(S)
Isopropyl Alcohol 70% v/v.
Sani-ultra Wipes
FDA Label NDC 78183-020
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Kunming Ansheng Industry & Trade Co., Ltd. for the product Sani-ultra Wipes (NDC 78183-020). 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(s), purpose, use, warnings, do not use, otc - when using, otc - stop use, otc - 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
Purpose
Antibacterial;
Use
Hand Sanitizer to reduce bacteria.
Warnings
For external use only.
Flammable. Keep away from fire or flame, heat, spark, electrical.
Do Not Use
Do not use on or around the eyes or damaged skin.
Otc - When Using
When using this product do not use in or contact the eyes, ears, and mouth.
Otc - Stop Use
Stop use and ask a doctor if irritation occurs.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. Contact medical help or poison control immediatedly, if swallowed.
Directions
- Open flip top when in use, pull out one wipe at a time for use.
- Close after use to prevent wipes from drying out.
Inactive Ingredients
Pure water
Package Label - Principal Display Panel
100 wipes in 1 canister.
NDC: 78183-020-01;
Sani (Sani 100p)
* Please review the disclaimer below.
