FELIX Hand Sanitizer Gel
- Manufacturer
- Ester Co., Ltd.
- Effective date
- 2020-05-21
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 23:14:05
Label at a glance#
ProductFELIX Hand Sanitizer Gel
Active ingredientALCOHOL
Label structure1 sections
Label contents#
Full prescribing information#
DailyMed RxNorm Mappings#
Product Linked Resources#
| Resource | Code type | Value | Equivalent identifiers | Source image |
|---|---|---|---|---|
| Barcode | EAN-13 | 8809563705795 | GTIN-13: 8809563705795 EAN-13: 8809563705795 GTIN storage (14 digits): 08809563705795 | FELIX 500 mL.jpg |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 74004-702-01 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-f294-a426-e053-dadaa90af4c2 | [Ester Co., Ltd.-FELIX HAND SANITIZER GEL] 500 ml : BOTTLE+PUMP : 74004-702-01 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 74004-702-01 | FELIX Hand Sanitizer Gel | 500 mL in 1 BOTTLE, PUMP | GEL | 500 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- FELIX Hand Sanitizer Gel
- ALCOHOL
- ALLANTOIN
- GREEN TEA LEAF
- BUTYLENE GLYCOL
- EDETOL
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
- WATER
- ALOE ARBORESCENS LEAF
- GLYCERIN
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 74004-702 | 74004-702-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ALLANTOIN | 344S277G0Z | IACT |
| GREEN TEA LEAF | W2ZU1RY8B0 | IACT |
| BUTYLENE GLYCOL | 3XUS85K0RA | IACT |
| EDETOL | Q4R969U9FR | IACT |
| CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE | 0A5MM307FC | IACT |
| WATER | 059QF0KO0R | IACT |
| ALOE ARBORESCENS LEAF | 09TD8L5SQV | IACT |
| ALCOHOL | 3K9958V90M | ACTIB |
| GLYCERIN | PDC6A3C0OX | 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 |
|---|---|---|---|---|---|---|
| a62507d9-048c-139f-e053-2995a90a2bc9 | a6250431-e7ea-3df1-e053-2a95a90a1659 | 2020-05-21 | a62507d9-048c-139f-e053-2995a90a2bc9 a6250431-e7ea-3df1-e053-2a95a90a1659 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
