Sherbet
- Manufacturer
- Dharma Research, Inc.
- Effective date
- 2021-07-02
- Label type
- HUMAN PRESCRIPTION DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 20:37:19
Label at a glance#
ProductSherbet
Active ingredientSODIUM FLUORIDE
Label structure1 sections
Label contents#
Full prescribing information#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 53045-224-17 | Sherbet | 490 g in 1 BOTTLE | GEL | 490 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Sherbet
- Sodium Fluoride
- FLUORIDE ION
- CITRIC ACID MONOHYDRATE
- HYDROFLUORIC ACID
- MAGNESIUM ALUMINUM SILICATE
- PHOSPHORIC ACID
- POLYSORBATE 20
- POTASSIUM HYDROXIDE
- WATER
- SODIUM BENZOATE
- SACCHARIN SODIUM
- TITANIUM DIOXIDE
- .ALPHA.-TOCOPHEROL ACETATE
- XANTHAN GUM
- XYLITOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 53045-224 | 53045-224-17 |
Ingredients#
Every source-derived ingredient row is available through these pages.
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 |
|---|---|---|---|---|---|---|
| 834fb2f1-c8fe-497f-89c4-bfd88b352aab | dec4d14f-de62-4a22-9d46-b06a6bbc8eb2 | 2021-07-02 | 834fb2f1-c8fe-497f-89c4-bfd88b352aab dec4d14f-de62-4a22-9d46-b06a6bbc8eb2 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
