Indications and uses
Hand sanitizer for decreasing bacteria on skin
Royal-Plant Hand Sanitizer
- Manufacturer
- Dor Properties LLC.
- Effective date
- 2020-04-11
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 23:06:09
Label at a glance#
ProductRoyal-Plant Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections
Dosage and administration
Take appropriate amount onto your hand and spread it all the way to fingertips. Rub the contents until it dries.
Contacts and useful links#
Label contents#
Full prescribing information#
Active ingredient
Benzalkonium Chloride (0.13%)
Purpose
Antibacterial
Uses
Hand sanitizer for decreasing bacteria on skin
Warnings
For external use only
Do not use if you are allergic to any of the ingredients
When using this product avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water. avoid contact with broken, irritated, or itching skin. Do not puncture or incinerate.
Stop use and ask a doctor if irritation or redness develops and condition persists for more than 72 hours
If pregnant or breast- feeding, ask a health professional before use.
Keep out of reach of children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.
Directions
Take appropriate amount onto your hand and spread it all the way to fingertips. Rub the contents until it dries.
Inactive ingredient
Water, Ozone, Oxydants, Sodium Hypochlorite, Chlorine Dioxide, Sodium Chlorate
Royal-Plant Sanitizer
DailyMed RxNorm Mappings#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 74606-100-01 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-3a79-a426-e053-dadaa90af4c2 | Royal-Plant Hand Sanitizer |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 74606-100-01 | Royal-Plant Hand Sanitizer | 60 mL in 1 BOTTLE | LIQUID | 60 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Royal-Plant Hand Sanitizer
- Benzalkonium Chloride
- SODIUM CHLORATE
- OZONE
- CHLORINE DIOXIDE
- WATER
- BENZALKONIUM
- SODIUM HYPOCHLORITE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 74606-100 | 74606-100-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| SODIUM CHLORATE | T95DR77GMR | IACT |
| OZONE | 66H7ZZK23N | IACT |
| CHLORINE DIOXIDE | 8061YMS4RM | IACT |
| WATER | 059QF0KO0R | IACT |
| BENZALKONIUM CHLORIDE | F5UM2KM3W7 | ACTIB |
| SODIUM HYPOCHLORITE | DY38VHM5OD | 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 |
|---|---|---|---|---|---|---|
| a3016af5-0919-7ac0-e053-2a95a90adf56 | a3016b07-ca42-7229-e053-2a95a90a50ef | 2020-04-11 | Warnings | a3016af5-0919-7ac0-e053-2a95a90adf56 a3016b07-ca42-7229-e053-2a95a90a50ef |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.