Label
Product Label (6450 Expresswipeshandsanitizer Qs)
Express Wipes Hand Sanitizer Liquid
FDA Label NDC 67858-645
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Questspecialty Corporation for the product Express Wipes Hand Sanitizer (NDC 67858-645). 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 label, otc - active ingredient, otc - ask doctor, otc - do not use, warnings, otc - keep out of reach of children, storage and handling, inactive ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Active Ingredient
Active Ingredient Purpose
Ethyl Alcohol 70%...... Antiseptic
Otc - Ask Doctor
Stop use and ask a doctor if irritation and redness develop. If condition persists for more than 72 hours consulta a doctor.
Otc - Do Not Use
Do not use in the eyes.
Warnings
Flammable. Keep awaay from fire or flame.
For external use only.
Otc - Keep Out Of Reach Of Children
Keep out of reah of children. If swallowed, get medical help or contact a Poison Cotnrol Center righ away.
Storage And Handling
- Store below 110 oF (43 oC).
Inactive Ingredient
Water, Propylene Glycol, Undeceth-7, Isopropyl Myristate, Aloe Barbacdensis Leaf Juice, Methyl Salicylae, Tocophenyl Aceate (Vitamin E).
Indications & Usage
- For handwashing to decrease bacterial on the skin.
- After changing diapers.
- After assisting ill persons.
- Before contact with a person under medical care or treatment.
- Recommended for repeat use.
Dosage & Administration
- Wet hands thoroughly with product and allow to dry.,
- Children under six years of age shoudl be supervised when using this product.
Otc - Purpose
Antiseptic
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