Moxe Citrus Splash Hand Sanitizer
- Manufacturer
- Premark Health Science
- Effective date
- 2025-04-30
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-06-01 01:00:08
Label at a glance#
ProductMoxe Citrus Splash Hand Sanitizer
Active ingredientALCOHOL
Label structure1 sections
Label contents#
Full prescribing information#
DailyMed RxNorm Mappings#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 84004-001-32 | Moxe Citrus Splash Hand Sanitizer | 946 mL in 1 BOTTLE, PLASTIC | GEL | 946 | 2 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Moxe Citrus Splash Hand Sanitizer
- Alcohol
- MANDARIN OIL
- ALOE
- .ALPHA.-TOCOPHEROL ACETATE, DL-
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
- GLYCERIN
- WATER
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 84004-001 | 84004-001-32 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ALCOHOL | 3K9958V90M | ACTIB |
| MANDARIN OIL | NJO720F72R | IACT |
| ALOE | V5VD430YW9 | IACT |
| .ALPHA.-TOCOPHEROL ACETATE, DL- | WR1WPI7EW8 | IACT |
| CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE | 0A5MM307FC | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| 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 |
|---|---|---|---|---|---|---|
| Moxe Citrus Splash Hand Sanitizer | ALCOHOL | Premark Health Science | 21f246d0-9133-efec-e063-6294a90aa219 | 2025-04-30 | Warnings | 84004-001-32 84004-001 84004000132 34045263-a2c9-2cf6-e063-6394a90af5f5 21f246d0-9133-efec-e063-6294a90aa219 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
