Dosage and administration
Wet hands thoroughly with product ant rise at the end.
Key Dermolac
- Manufacturer
- Key Química S.A. de C.V. | Cyan Labs S.A. de C.V.
- Effective date
- 2025-01-07
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-06-01 00:51:04
Label at a glance#
ProductKey Dermolac
Active ingredientLACTIC ACID, L-
Label structure10 sections
Label contents#
Full prescribing information#
Active ingredients
- L-(+)-lactic acid 1.6 %
Purpose
Antiseptic
Do not use
Do not use this product in or near the eyes.
OTC - STOP USE SECTION
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 SECTION
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.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed Product Concepts#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 58345-105-01 | Key Dermolac | 800 mL in 1 BAG | LIQUID | 800 | 2 | |
| 58345-105-01 | Key Dermolac | 3 in 1 BOX | LIQUID | 3 | 2 | |
| 58345-105-02 | Key Dermolac | 4000 mL in 1 BOTTLE | LIQUID | 4000 | 2 | |
| 58345-105-02 | Key Dermolac | 4 in 1 BOX | LIQUID | 4 | 2 | |
| 58345-105-03 | Key Dermolac | 4000 mL in 1 BOTTLE, PUMP | LIQUID | 4000 | 2 | |
| 58345-105-03 | Key Dermolac | 4 in 1 BOX | LIQUID | 4 | 2 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Key Dermolac
- Jabon antiseptico a base de acido lactico
- WATER
- SODIUM LAURETH SULFATE
- DIRECT RED 81
- SODIUM HYDROXIDE
- COCAMIDOPROPYL BETAINE
- LACTIC ACID, L-
- SODIUM CHLORIDE
- EDETATE SODIUM
- CARMOISINE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 58345-105 | 58345-105-01, 58345-105-02, 58345-105-03 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| WATER | 059QF0KO0R | IACT |
| SODIUM LAURETH SULFATE | BPV390UAP0 | IACT |
| DIRECT RED 81 | 7E49Q56PNB | IACT |
| SODIUM HYDROXIDE | 55X04QC32I | IACT |
| COCAMIDOPROPYL BETAINE | 5OCF3O11KX | IACT |
| LACTIC ACID, L- | F9S9FFU82N | ACTIB |
| SODIUM CHLORIDE | 451W47IQ8X | IACT |
| EDETATE SODIUM | MP1J8420LU | IACT |
| CARMOISINE | DR4641L47F | IACT |
Source Document#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Key Dermolac | JABON ANTISEPTICO A BASE DE ACIDO LACTICO | Key Qumica S.A. de C.V. | 1c368292-4c33-8488-e063-6294a90a0fa9 | 2025-01-07 | Warnings | 58345-105-03 58345-105-02 58345-105-01 58345-105 58345010502 58345010503 58345010501 2b26c2ec-601b-7dd5-e063-6294a90aaaa7 1c368292-4c33-8488-e063-6294a90a0fa9 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.