Mova Liquid Hand Antibacterial
FDA Label NDC 81235-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Mova Chemical S.a for the product Mova Liquid Hand Antibacterial (NDC 81235-001). 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, purpose, use, warnings, do not use, keep out of reach of children, directions for use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Benzalkonium Chloride 0.13%
Purpose
Antiseptic
Use
Antiseptic liquid hand soap to help decrease bacteria on the skin.
Recommended for repeated use.
Warnings
- Allergy alert DOES NOT contain essential almond oil.
Do Not Use
- on intimate parts of the body.
- Use for hand washing only.
Keep Out Of Reach Of Children
Avoid contact with eyes. In case of eye contact, flush with water. If swallowed, get medical help or contact a Poison Control Center.
Directions For Use
- Wet hands with water-lather vigorously and wash skin-rinse and dry thoroughly.
- For home and institutional use
Other Information
- Store at room temperature no higher than 45°C (113°F) Avoid direct sunlight.
- Keep in closed containers, free from direct sunlight.
Inactive Ingredients
Triethanolamine (TEA), Glycerin USP, Probethaine PB-12, Methylether PPG-2, Methylisothiazoline, Tetrasodium EDTA, Citric Acid, Almond Fragrance, Glycol Distearate.
Question Or Coments?
- Call USA +512-853-9176 Monday through Friday 8:00am to 4:30pm CST.
- Call Panama +507 831-1181 Monday through Friday 8:00am to 4:30pm CST.
Package Labeling:
Label3 (Label3)
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