Indications and uses
For hand sanitizing to decrease bacteria Recommended for repeated use
HAND SANITIZER
- Manufacturer
- Skywash International
- Effective date
- 2021-09-22
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 4
- Source
- full-release
- Hydrated at
- 2026-05-31 23:42:28
Label at a glance#
ProductHAND SANITIZER
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections
Dosage and administration
Spray a small amount 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
- Recommended for repeated use
WARNINGS
For extrenal 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 imitation 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
Spray a small amount into palm of hand
- Rub thoroughly over all surfaces of both hands
- Rub hands together briskly until dry.
INACTIVE INGREDIENTS
water, cetrimonium chloride, laurtrimonium chloride, dihydroxyethyl cocamine oxide, glycereth–17 cocoate, citric acid, lavender 4042, Eucalyplus 80/85.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed RxNorm Mappings#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 78987-101-11 | 2022-07-29 | C162847 | 48780-1 | e4f33bdf-a94f-d8a0-e053-dadaa90a6e4e | SKYWASH - PURIFYING HAND SANITIZER - 0.1% BKC |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 78987-101-11 | HAND SANITIZER | 238 mL in 1 BOTTLE, SPRAY | SPRAY | 238 | 4 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- HAND SANITIZER
- BENZALKONIUM CHLORIDE
- WATER
- CETRIMONIUM CHLORIDE
- LAURTRIMONIUM CHLORIDE
- DIHYDROXYETHYL COCAMINE OXIDE
- GLYCERETH-17 COCOATE
- ANHYDROUS CITRIC ACID
- LAVENDER OIL
- EUCALYPTUS OIL
- BENZALKONIUM
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 78987-101 | 78987-101-11 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| WATER | 059QF0KO0R | IACT |
| CETRIMONIUM CHLORIDE | UC9PE95IBP | IACT |
| LAURTRIMONIUM CHLORIDE | A81MSI0FIC | IACT |
| DIHYDROXYETHYL COCAMINE OXIDE | 8AR51R3BL5 | IACT |
| GLYCERETH-17 COCOATE | 3057VPT0KC | IACT |
| ANHYDROUS CITRIC ACID | XF417D3PSL | IACT |
| LAVENDER OIL | ZBP1YXW0H8 | IACT |
| EUCALYPTUS OIL | 2R04ONI662 | IACT |
| BENZALKONIUM CHLORIDE | F5UM2KM3W7 | ACTIB |
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 |
|---|---|---|---|---|---|---|
| cc9d5718-4bdb-8812-e053-2995a90ad705 | 5bdccb8c-4ea7-47da-a774-f9cd29d7111c | 2021-09-22 | Warnings | cc9d5718-4bdb-8812-e053-2995a90ad705 5bdccb8c-4ea7-47da-a774-f9cd29d7111c |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.