Freshen Up
- Product NDC
- 77782-005
- 11-digit product format
- 777820005
- Labeler code
- 77782
- Product ID
- 77782-005_476f4542-d1f1-153a-e063-6294a90a3e6c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SODIUM FLUORIDE, POTASSIUM NITRATE
- Dosage form
- GEL, DENTIFRICE
- Route
- DENTAL
- Labeler
- MKJ BRANDS LLC
- Application
- M021
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-01-02
- Substance
- SODIUM MONOFLUOROPHOSPHATE
- Active strength
- .76 g/100g
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Freshen Up
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM MONOFLUOROPHOSPHATE | .76 g/100g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | C810JCZ56Q |
| Rxcui | 545626 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 77782-005-20 | Freshen Up | 2 in 1 BOX | GEL, DENTIFRICE | 2 | | 1 |
| 77782-005-20 | Freshen Up | 99 g in 1 BOTTLE | GEL, DENTIFRICE | 99 | | 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 |
|---|
| 77782-005-20 | 77782000520 | 2 BOTTLE in 1 BOX (77782-005-20) / 99 g in 1 BOTTLE | 2 bottle | 2026-01-02 | No | No | Current |