Plak Smacker
- Product NDC
- 72796-0412
- 11-digit product format
- 727960412
- Labeler code
- 72796
- Product ID
- 72796-0412_42c89f0a-b4bb-a17b-e063-6294a90a09bf
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Stannous Fluoride
- Dosage form
- GEL
- Route
- DENTAL; ORAL
- Labeler
- Young Innovations, Inc.
- Application
- M021
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2007-12-31
- Substance
- STANNOUS FLUORIDE
- Active strength
- .969 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Plak Smacker
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| STANNOUS FLUORIDE | .969 mg/g |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| 3FTR44B32Q | Internal UNII lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| e65c62d9-e8a6-3101-e053-2995a90a1494 | Available on FDA.report |
FDA-Initiated Inactive NDC Indexing#
| Effective | Related label |
|---|---|
| 2024-02-06 | Plak Smacker Stannous Gel - Bubble Gum |
| 2024-02-06 | Plak Smacker Stannous Gel - Bubble Gum |
| 2024-01-30 | Plak Smacker Stannous Gel - Bubble Gum |
| 2024-01-30 | Plak Smacker Stannous Gel - Bubble Gum |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 72796-0412-1 | Plak Smacker | 121.9 g in 1 TUBE | GEL | 121.9 | 3 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 72796-0412 | PLAK SMACKER (STANNOUS FLUORIDE) GEL [YOUNG INNOVATIONS, INC.] | 2 | Current NDC, Legacy NDC, 1 package rows | 20240207_e65c62d9-e8a6-3101-e053-2995a90a1494.zip |
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 |
|---|---|---|---|---|---|---|
| Anticavity | SODIUM FLUORIDE | Old East Main Co. | 64f3d92d-f58c-4bc2-8819-f91492221ddb | 2026-03-02 | Warnings, Adverse reactions | M021 |
| Anticavity | SODIUM FLUORIDE | Old East Main Co. | c7b9e9cd-3cf7-4657-83c9-e221e1c35977 | 2026-03-02 | Warnings, Adverse reactions | M021 |
| Instant Whitening | INSTANT WHITENING TOOTHPASTE | Guangzhou City Caiye Cosmetics CO., Ltd | 2807ece8-a1a5-b626-e063-6394a90aac62 | 2026-03-02 | Warnings | M021 |
| Coffe Tea Stain Remover Tooth | COFFE TEA STAIN REMOVER TOOTHPASTE | Guangzhou City Caiye Cosmetics CO., Ltd | 2845d7af-7a0b-9bc8-e063-6294a90ac8b3 | 2026-03-02 | Warnings | M021 |
| Professional whitening tooth | PROFESSIONAL WHITENING TOOTHPASTE | Guangzhou City Caiye Cosmetics CO., Ltd | 291eba71-14da-fac3-e063-6294a90aa3cc | 2026-03-02 | Warnings | M021 |
| purple tooth | PURPLE TOOTHPASTE | Guangzhou City Caiye Cosmetics CO., Ltd | 291f0312-238c-71d5-e063-6294a90a39e1 | 2026-03-02 | Warnings | M021 |
| Professional Choice | PROFESSIONAL CHOICE TOOTHPASTE | Guangzhou City Caiye Cosmetics CO., Ltd | 28406739-6a8c-1ce8-e063-6394a90a08f8 | 2026-03-02 | Warnings | M021 |
| Anticavity | SODIUM FLUORIDE | The Kroger Co. | 27a98b64-8369-4f3d-b487-d7ce98abc69f | 2026-02-27 | Warnings, Adverse reactions | M021 |
| Anticavity | SODIUM FLUORIDE | The Kroger Co. | 390dd1b5-2dd1-4b55-b4b3-e441ada61238 | 2026-02-27 | Warnings, Adverse reactions | M021 |
| Alcohol-Free Anticavity | SODIUM FLUORIDE | The Kroger Co. | 5459eeee-adf0-4afe-b190-62d4fa113806 | 2026-02-27 | Warnings, Adverse reactions | M021 |
| Oral Antivavity | SODIUM FLUORIDE | The Kroger Co. | 932723b8-9875-4f37-8c11-018c94ae0ae1 | 2026-02-27 | Warnings, Adverse reactions | M021 |
| Anticavity | SODIUM FLUORIDE | The Kroger Co. | d0c552d8-44ad-4d95-b3fb-17015f44b334 | 2026-02-27 | Warnings, Adverse reactions | M021 |
| Anticavity Rinse | SODIUM FLUORIDE | Walmart Inc. | 3beb65e4-ae8e-4e51-b9ba-181cbec41eff | 2026-02-27 | Warnings, Adverse reactions | M021 |
| Anticavity | SODIUM FLUORIDE | Walmart Inc. | 61669087-0af6-4192-b514-afcfe7d8ba98 | 2026-02-27 | Warnings, Adverse reactions | M021 |
| Anticavity | SODIUM FLUORIDE | Walmart Inc. | e79e43e6-d6b6-4df4-9d9f-fe9fe35f180d | 2026-02-27 | Warnings, Adverse reactions | M021 |
| Alcohol-Free Anticavity | SODIUM FLUORIDE | Walmart Inc. | 1fd2f3ca-066e-282a-e063-6294a90a05a9 | 2026-02-27 | Warnings, Adverse reactions | M021 |
| Anticavity | SODIUM FLUORIDE | Walmart Inc. | af5b93e7-5cce-4e01-8df2-54494d8b2910 | 2026-02-27 | Warnings, Adverse reactions | M021 |
| Anticavity | SODIUM FLUORIDE | Walmart Inc. | 4590ca97-130c-46b2-9ba0-38f4703ef30a | 2026-02-27 | Warnings, Adverse reactions | M021 |
| Colgate Anticavity | SODIUM MONOFLUOROPHOSPHATE | MING FAI ENTERPRISE (CAMBODIA) CO., LTD. | 4ba81636-cdb7-e904-e063-6394a90a8bd5 | 2026-02-25 | Warnings | M021 |
| Anticavity Rinse | SODIUM FLUORIDE | Family Dollar Stores, Inc | 32a92add-c9db-4733-8e35-613825fdf081 | 2026-02-24 | Warnings, Adverse reactions | M021 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 72796-0412-1 | 72796041201 | 121.9 g in 1 TUBE (72796-0412-1) | 121.9 g | 2007-12-31 | 0000-00-00 | No | No | Current |