Indications and uses
Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.
Hand Sanitizer
- Manufacturer
- The Source Design Collections
- Effective date
- 2021-04-16
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-05-31 23:39:44
Label at a glance#
ProductHand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure12 sections
Dosage and administration
Place enough product on hands to cover all surfaces.Rub hands together until dry.
Storage and handling
Store in a cool dry place, away from direct sunlight and heat.
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Benzalkonium Chloride 0.13%
OTC - PURPOSE SECTION
Antiseptic
Uses
Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.
INACTIVE INGREDIENT SECTION
Water (aqua), propylene glycol, phenoxyethanol,fragrance (parfum), hydroxyethylcellulose, alcohol, linalool.
Directions
Place enough product on hands to cover all surfaces.Rub hands together until dry.
WARNINGS SECTION
For external use only.
OTC - DO NOT USE SECTION
Do not use on open skin wounds or children under 2 months of age.
OTC - WHEN USING SECTION
When using this product keep out of eyes,ears, and mouth. ln case of contact with eyes,rinse eyes thoroughly with water.
OTC - STOP USE SECTION
Stop use and ask a doctor if irritation or rash occurs.These may be signs of a serious condition.
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 immediately.
Other information
Store in a cool dry place, away from direct sunlight and heat.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed RxNorm Mappings#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 81726-006-01 | 2022-07-29 | C162847 | 48780-1 | e4f33bdf-af84-d8a0-e053-dadaa90a6e4e | bfbe7f95-c4e7-7ec0-e053-2995a90a1942 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 81726-006-01 | Hand Sanitizer | 95 mL in 1 BOTTLE | GEL | 95 | 2 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Hand Sanitizer
- FRAGRANCE EUCALYPTUS SPEARMINT ORC1601627
- BENZALKONIUM CHLORIDE
- BENZALKONIUM
- WATER
- HYDROXYETHYL CELLULOSE, UNSPECIFIED
- PHENOXYETHANOL
- ALCOHOL
- PROPYLENE GLYCOL
- LINALOOL, (+/-)-
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 81726-006 | 81726-006-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| FRAGRANCE EUCALYPTUS SPEARMINT ORC1601627 | E90O5M6HMB | IACT |
| BENZALKONIUM CHLORIDE | F5UM2KM3W7 | ACTIB |
| WATER | 059QF0KO0R | IACT |
| HYDROXYETHYL CELLULOSE, UNSPECIFIED | T4V6TWG28D | IACT |
| PHENOXYETHANOL | HIE492ZZ3T | IACT |
| ALCOHOL | 3K9958V90M | IACT |
| PROPYLENE GLYCOL | 6DC9Q167V3 | IACT |
| LINALOOL, (+/-)- | D81QY6I88E | 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 |
|---|---|---|---|---|---|---|
| c01101b4-8d69-66f7-e053-2a95a90a3c77 | bfbe7f95-c4e7-7ec0-e053-2995a90a1942 | 2021-04-16 | Warnings | c01101b4-8d69-66f7-e053-2a95a90a3c77 bfbe7f95-c4e7-7ec0-e053-2995a90a1942 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.