Indications and uses
For hand sanitizing to decrease bacteria on the skin. Recommended for repeated use.
Foaming Hand Sanitizer
- Manufacturer
- Theochem Laboratories Inc
- Effective date
- 2013-12-13
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 22:37:50
Label at a glance#
ProductFoaming Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections
Dosage and administration
Pour contents into the Foaming Dispenser reservoir. For first use applications, pump dispenser a few time to prime. Pump a small amount of foam into palm of hand. Rub thoroughly over all surfaces of both hands. Rub hands together briskly until dry.
Label contents#
Full prescribing information#
Active Ingredient
Benzalkonium Chloride 0.1%
Purpose
Antimicrobial
Uses
For hand sanitizing to decrease bacteria on the skin.
Recommended for repeated use.
Warnings
For external use only.
When using this product, avoid contact with eyes. In case of eye contact, flush eyes with water.
Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours.
Keep out of reach of children
If swallowed, get medical help or contact a Poison Control Center right away.
Directions:
Pour contents into the Foaming Dispenser reservoir. For first use applications, pump dispenser a few time to prime. Pump a small amount of foam into palm of hand. Rub thoroughly over all surfaces of both hands. Rub hands together briskly until dry.
Other Information
Store below 110 °F (43 °C). May discolor certain fabrics or surfaces.
Inactive Ingredients
Water, dihydroxypropyl PEG-5 linoleammonium chloride, glycereteh-2 cocoate, behentrimonium chloride, dihydroxyethyl cocamine oxide, aloe barbadensis leaf juice.
PRINCIPAL DISPLAY PANELFOAMING HAND SANITIZER NET CONTENTS: 3.785 LITERS
DailyMed RxNorm Mappings#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 68878-119-11 | 2019-11-27 | C162847 | 48780-1 | 9855e2a2-38c4-60a7-e053-dbdaa90a05bd | Foaming Hand Santizer |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 68878-119-11 | Foaming Hand Sanitizer | 3785 mL in 1 BOTTLE, PLASTIC | LIQUID | 3785 | 1 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| BENZALKONIUM CHLORIDE | ACTIVE INGREDIENT | F5UM2KM3W7 | 1 | |
| BENZALKONIUM | ACTIVE MOIETY | 7N6JUD5X6Y | 1 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | 1 |
Products#
Every source-derived product name is available through these pages.
- Foaming Hand Sanitizer
- BENZALKONIUM CHLORIDE
- BENZALKONIUM
- WATER
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 68878-119 | 68878-119-11 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| BENZALKONIUM CHLORIDE | F5UM2KM3W7 | ACTIB |
| WATER | 059QF0KO0R | 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 |
|---|---|---|---|---|---|---|
| 518ac54d-fdd1-4eda-ab42-8818bb33d176 | e8177cff-3581-4d5a-943d-2c4ea7bc7a44 | 2013-12-13 | Warnings | 518ac54d-fdd1-4eda-ab42-8818bb33d176 e8177cff-3581-4d5a-943d-2c4ea7bc7a44 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.