AZX Wellness Hand Sanitizer
AZX Wellness Hand Sanitizer is an FDA drug label for the active ingredient ALCOHOL manufactured by ASC Marketing LTD administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20231201.
Generic: ALCOHOL
Manufacturer: ASC Marketing LTD
Product Type: HUMAN OTC DRUG
Route: TOPICAL
Dosage Form:
NDC: 73145-007
Application: 505G(a)(3)
Effective: 20231201
Active Ingredients: Active Ingredients: Ethyl Alcohol 80% Purpose: Antiseptic
Indications & Usage
USES For hand washing to decrease bacteria on the skin.
Dosage & Administration
DIRECTIONS Wet hands thoroughly for at least 20 seconds with product and allow to dry without wiping. Supervise children in the use of this product.
Contraindications
Not available.
Warnings
WARNINGS For external use only. Flammable. Keep away from fire or flames. Do not use in the eyes. In case of contact, rinse eyes thoroughly with water. Stop use and ask a doctor if irritation or redness develop and persist for more than 72 hours. Keep out of reach of children. If swallowed get medical help or contact Poison Control Center right away. Store between 59-86°F (15-30°C). Avoid freezing and excessive heat above 104°F (40°C).
Adverse Reactions
Not available.
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