OTC - ACTIVE INGREDIENT SECTION
Benzalkonium Chloride 0.13%
Anti-microbial Alcohol Free Hand Sanitizer
- Manufacturer
- Ultra Chem Labs | Ultra Chem Labs, Corp
- Effective date
- 2020-08-04
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-05-31 23:23:45
Label at a glance#
ProductAnti-microbial Alcohol Free Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure11 sections
Label contents#
Full prescribing information#
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
OTC - STOP USE SECTION
Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours.
OTC - WHEN USING SECTION
When using this product avoid contact with eyes. In case of eye contact, flush eyes with water
OTHER SAFETY INFORMATION
Directions • Pump a small amount of foam into palm of hand • Rub thoroughly over all surfaces of both hands for 15 seconds • Rinse with potable water
INACTIVE INGREDIENT SECTION
Inactive ingredients Water, laurtrimonium chloride, alkyl polyglucoside, uv indicator cocamidopropylamine oxide, alkyl polyglycoside, citric acid
WARNINGS SECTION
Warnings
For external use only
DOSAGE & ADMINISTRATION SECTION
Pump a small amount of foam into palm of hand • Rub thoroughly over all surfaces of both hands for 15 seconds • Rinse with potable water
INDICATIONS & USAGE SECTION
• For hand washing to decrease bacteria on the skin
• Recommended for repeated use
OTC - PURPOSE SECTION
Antimicrobial
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 79208-001-01 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-c6a7-a426-e053-dadaa90af4c2 | a84ec7b9-121c-498a-e053-2995a90a900b |
| 79208-001-32 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-c6a7-a426-e053-dadaa90af4c2 | a84ec7b9-121c-498a-e053-2995a90a900b |
| 79208-001-50 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-c6a7-a426-e053-dadaa90af4c2 | a84ec7b9-121c-498a-e053-2995a90a900b |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 79208-001-01 | Anti-microbial Alcohol Free Hand Sanitizer | 3785 mg in 1 BOTTLE | LIQUID | 3785 | 2 | |
| 79208-001-32 | Anti-microbial Alcohol Free Hand Sanitizer | 946 mg in 1 BOTTLE | LIQUID | 946 | 2 | |
| 79208-001-50 | Anti-microbial Alcohol Free Hand Sanitizer | 50 mg in 1 BOTTLE | LIQUID | 50 | 2 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Anti-microbial Alcohol Free Hand Sanitizer
- Benzalkonium Chloride
- BENZALKONIUM
- ANHYDROUS CITRIC ACID
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 79208-001 | 79208-001-50, 79208-001-32, 79208-001-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| BENZALKONIUM CHLORIDE | F5UM2KM3W7 | ACTIB |
| ANHYDROUS CITRIC ACID | XF417D3PSL | 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 |
|---|---|---|---|---|---|---|
| ac14846e-41f3-37c4-e053-2a95a90a3cdd | a84ec7b9-121c-498a-e053-2995a90a900b | 2020-08-04 | Warnings | ac14846e-41f3-37c4-e053-2a95a90a3cdd a84ec7b9-121c-498a-e053-2995a90a900b |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.