Lubrima
FDA Label NDC 80481-101
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Agro Grup Teknoloji Bilgisayar Sistemleri Temizlik Maddeleri Sanayi Ve Ticaret Limited Sir for the product Lubrima (NDC 80481-101). 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, warnings, directions, other information, inactive ingredients, packaging, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Ethyl Alcohol (80%)
Purpose
Hand Sanitizing
Warnings
Ask a doctor before use if you have
• glaucoma
• a breathing problem such as emphysema or chronic bronchitis
Do NOT dispose in toilet to avoid clogging. Keep in cool place indoors avoid high temperature and direct sunlight. Do NOT throw on fire.
If pregnant or breast-feeding, ask a health professional before use.
Directions
Open the cover of the wet wipes or seal the sticker. After use please close the wet wipes cover or seal the sticker to keep the wet wipes moist.
| adults and children 12 years and over | Use as directed |
| children 6 years to under 12 years | Use as directed |
| children under 6 years | ask a doctor |
Other Information
• store at 20-25° C (68-77° F)
• protect from excessive moisture
Inactive Ingredients
Aqua, Glycerine
Packaging
Image (8048110 101)
Image (80481101 01)
* Please review the disclaimer below.
