EverSmile Squirt
- Product NDC
- 72655-702
- 11-digit product format
- 726550702
- Labeler code
- 72655
- Product ID
- 72655-702_3bb09e05-affd-4102-a8b0-c37120d979ba
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Fluoride 0.05%
- Dosage form
- LIQUID
- Route
- DENTAL
- Labeler
- Everbrands, Inc.
- Application
- M021
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-04-10
- Substance
- SODIUM FLUORIDE
- Active strength
- .05 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- EverSmile Squirt
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM FLUORIDE | .05 g/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 8ZYQ1474W7 |
| Rxcui | 240698 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72655-702-01 | EverSmile Squirt | 100 mL in 1 BOTTLE, PUMP | LIQUID | 100 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72655-702-01 | 72655070201 | 100 mL in 1 BOTTLE, PUMP (72655-702-01) | 100 ml | 2026-04-10 | No | No | Historical |