Welamd Maximum Strength Antibacterial Hand Sanitizer
FDA Label NDC 80595-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Avp Labs And Investment Group Llc for the product Welamd Maximum Strength Antibacterial Hand Sanitizer (NDC 80595-001). 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 drug facts, active ingredient (by volume), purpose, use[s], warnings:, do not use:, when using this product:, stop use:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient (By Volume)
Ethyl alcohol 70%
Purpose
Antiseptic
Use[S]
Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.
Warnings:
For external use only. Flammable, keep away from fire or flame.
Do Not Use:
- on children less than 2 months of age
- on open wounds
When Using This Product:
keep out of eyes, ears and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop Use:
if irritation or rash occurs. These may be signs of a serious condition.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions:
Put enough product on hands to cover surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to
avoid swallowing.
Other Information:
Store between 15˚-30˚C (59˚-86˚F). Avoid Freezing and excessive heat above 40˚C (104˚F)
Inactive Ingredients:
Carbomer,Glycerine, Triethanolamine, Water
Package Labeling:
Bottle (Bottle)
Bottle2 (Bottle2)
* Please review the disclaimer below.
