POP Gel Whatzzup Watermelon
- Product NDC
- 53208-582
- 11-digit product format
- 532080582
- Labeler code
- 53208
- Product ID
- 53208-582_2c6bed6a-e21e-0073-e063-6394a90a28b1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Fluoride
- Dosage form
- PASTE, DENTIFRICE
- Route
- DENTAL
- Labeler
- LG H&H Co., Ltd.
- Application
- M021
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-09-18
- Substance
- SODIUM FLUORIDE
- Active strength
- 1.3 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- POP Gel Whatzzup Watermelon
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM FLUORIDE | 1.3 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 8ZYQ1474W7 |
| Rxcui | 891775 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 53208-582-60 | POP Gel Whatzzup Watermelon | 160 g in 1 TUBE | PASTE, DENTIFRICE | 160 | | 2 |
| 53208-582-60 | POP Gel Whatzzup Watermelon | 1 in 1 CARTON | PASTE, DENTIFRICE | 1 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53208-582 | POP GEL WHATZZUP WATERMELON (SODIUM FLUORIDE) PASTE, DENTIFRICE [LG H&H CO., LTD.] | 2 | Current NDC, 2 package rows | 20250125_05b276a1-3778-104d-e063-6294a90a7537.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 53208-582-60 | 53208058260 | 1 TUBE in 1 CARTON (53208-582-60) / 160 g in 1 TUBE | 1 tube | 2023-09-18 | No | No | Historical |