Dosage and administration
Wet hands thoroughly with product and allow to dry without wiping.
Wet hands thoroughly with product and allow to dry without wiping.
Drug Facts
Alcohol 75% (v/v)
Antiseptic
Water (Aqua), PEG-6 Caprilic/Capric Glycerides, Shea Butteramidopropyl Betaine, Disodium Lauriminodipropionate Tocopheryl Phosphates, Sodium Lactate, PEG/PPG-25/25 Dimethicone, Lactic Acid, PEG-14M
1-800-347-9800 Mon–Fri, 8 AM–5 PM EST
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 444b3e50-f226-46ef-bfca-2e7035d140cd | Product name | 1 | 20190611 |
| 597b1cfd-7b31-5048-62be-ca5cd740da2f | Product name | 1 | 20140508 |
| ec2149b3-5c6d-5344-f757-c86411073075 | Product name | 1 | 20140508 |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 65321-024-04 | Foam Hand Sanitizer | 1000 mL in 1 POUCH | LIQUID | 1000 | 6 |
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| Alcohol | ACTIVE INGREDIENT | 3K9958V90M | 3 | |
| Alcohol | ACTIVE MOIETY | 3K9958V90M | 3 | |
| Lactic Acid | INACTIVE INGREDIENT | 33X04XA5AT | 3 | |
| Sodium Lactate | INACTIVE INGREDIENT | TU7HW0W0QT | 3 | |
| Water | INACTIVE INGREDIENT | 059QF0KO0R | 3 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 65321-024 | 65321-024-04 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ALCOHOL | 3K9958V90M | ACTIB |
| WATER | 059QF0KO0R | IACT |
| SODIUM LACTATE | TU7HW0W0QT | IACT |
| LACTIC ACID, UNSPECIFIED FORM | 33X04XA5AT | IACT |
Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.
| DailyMed ingredient | IID ingredient | UNII | Dosage form / route | Potency | Maximum daily exposure | Match |
|---|---|---|---|---|---|---|
| Lactic Acid | LACTIC ACID | 33X04XA5AT | CREAM / VAGINAL | 0.81 %w/w | ||
| Lactic Acid | LACTIC ACID | 33X04XA5AT | CAPSULE / ORAL | 132 mg | ||
| Lactic Acid | LACTIC ACID | 33X04XA5AT | INJECTION / INTRAVENOUS | 2232 mg | ||
| Lactic Acid | LACTIC ACID | 33X04XA5AT | SUSPENSION / TOPICAL | 0.7 %w/w | ||
| Sodium Lactate | SODIUM LACTATE | TU7HW0W0QT | GEL / TOPICAL | 4 mg | ||
| Lactic Acid | LACTIC ACID | 33X04XA5AT | CONCENTRATE / ORAL | 50 mg/5ml | ||
| Lactic Acid | LACTIC ACID | 33X04XA5AT | GEL / TOPICAL | 30 mg | ||
| Sodium Lactate | SODIUM LACTATE | TU7HW0W0QT | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / INTRAVENOUS | 18.7 mg | ||
| Sodium Lactate | SODIUM LACTATE | TU7HW0W0QT | SOLUTION / INTRAPERITONEAL | 0.45 %w/v | ||
| Lactic Acid | LACTIC ACID | 33X04XA5AT | INJECTION, SOLUTION / INTRAVENOUS | 87 mg | ||
| Lactic Acid | LACTIC ACID | 33X04XA5AT | OINTMENT / TOPICAL | ADJ PH | ||
| Lactic Acid | LACTIC ACID | 33X04XA5AT | TABLET / ORAL | ADJ PH | ||
| Sodium Lactate | SODIUM LACTATE | TU7HW0W0QT | INJECTION, SOLUTION / INFILTRATION | 0.17 %v/v | ||
| Lactic Acid | LACTIC ACID | 33X04XA5AT | SOLUTION / ORAL | 192 mg | ||
| Lactic Acid | LACTIC ACID | 33X04XA5AT | CREAM / TOPICAL | 1 %w/w | ||
| Sodium Lactate | SODIUM LACTATE | TU7HW0W0QT | SUSPENSION / ORAL | 20 mg/1ml | ||
| Lactic Acid | LACTIC ACID | 33X04XA5AT | LOTION / TOPICAL | 5.7 %w/w | ||
| Lactic Acid | LACTIC ACID | 33X04XA5AT | INJECTION / INTRAMUSCULAR | 1.16 %w/v | ||
| Sodium Lactate | SODIUM LACTATE | TU7HW0W0QT | SOLUTION / TOPICAL | 0.93 %w/w | ||
| Sodium Lactate | SODIUM LACTATE | TU7HW0W0QT | INJECTION / INTRAVENOUS | 54 mg | ||
| Lactic Acid | LACTIC ACID | 33X04XA5AT | SOLUTION / TOPICAL | 7.22 %w/w | ||
| Lactic Acid | LACTIC ACID | 33X04XA5AT | INJECTION / SUBCUTANEOUS | 10 mg | ||
| Lactic Acid | LACTIC ACID | 33X04XA5AT | AEROSOL, FOAM / TOPICAL | 11 mg | ||
| Lactic Acid | LACTIC ACID | 33X04XA5AT | INJECTION / INTRACARDIAC | 0.01 %w/v | ||
| Lactic Acid | LACTIC ACID | 33X04XA5AT | SUPPOSITORY / VAGINAL | NA |
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 |
|---|---|---|---|---|---|---|
| e38e73ac-6c17-444c-806c-1157d3bab99d | 34b4405d-16fe-4e50-a2f1-026a55451a21 | 2026-06-16 | Warnings | 34b4405d-16fe-4e50-a2f1-026a55451a21 |
Adverse event summaries are temporarily unavailable. Other product information remains available.