Active Ingredients
- L-(+)-lactic acid 1.6 %
Key Dermolac Liquid
FDA Label NDC 58345-105
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Key Qu�mica S.a. De C.v. for the product Key Dermolac (NDC 58345-105). 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 active ingredients, purpose, do not use, otc - stop use, otc - keep out of reach of children, inactive ingredients, directions, use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Do Not Use
Do not use this product in or near the eyes.
Otc - Stop Use
Stop use if irritation or redness develop. If conditions persist for more than 72 hours, consult a doctor.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, seek inmediate medical attention or call a poison center.
Inactive Ingredients
- Water
- Sodium Laureth Sulfate
- Sodium chloride
- Cocamidopropyl betaine
- Sodium hydroxide
- Tetrasodium EDTA
- Acid Red 14
- Direct Red 81
Directions
Wet hands thoroughly with product ant rise at the end.
Use
To decrease bacteria on skin that could cause diseases.
Warnings
- For external use only.
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