Active Ingredient(S)
Alcohol 80% v/v. Purpose: Antiseptic
Tizer Go Wipes
FDA Label NDC 80628-102
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 Pnr Group, Llc for the product Tizer Go Wipes (NDC 80628-102). 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
Antiseptic
Use
To help reduce bacteria on the skin that may cause disease.
Warnings
For external use only. Flammable. Keep away from heat or flame
Do Not Use
- in children less than 2 months of age
- on open skin wounds
Otc - When Using
When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
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. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Wipe hands thoroughly with towelette. Allow to dry. Discard after single use. For occasional and personal domestic use.
Other Information
Lot No. and Expiration Date can be found on container.
Inactive Ingredients
Water (Aqua), Propylene Glycol, Glycerin, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate
* Please review the disclaimer below.
