Dentemp Canker Cover
- Product NDC
- 73653-210
- 11-digit product format
- 736530210
- Labeler code
- 73653
- Product ID
- 73653-210_47e23f4e-d4a7-7af1-e063-6394a90a2f05
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Canker Cover
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL; TOPICAL
- Labeler
- DOC Brands
- Application
- M022
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-02-02
- Substance
- MENTHOL
- Active strength
- 2.5 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- 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
- Dentemp Canker Cover
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| MENTHOL | 2.5 mg/1 |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| L7T10EIP3A | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 2628246 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 2e7fbf9d-553c-c7bf-e063-6294a90a5f79 | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 6bd95106-a412-1dad-b9cc-4cb74bfb27ce | Product name | 2 | 20230315 |
| 7cda52fc-125f-421c-8fea-bc1974370c49 | Product name | 2 | 20180703 |
| d5e51f11-ad28-caa4-4b49-4143974782ad | Product name | 1 | 20150831 |
| 290f523a-f9db-9774-b5a9-e1f908ac1782 | Product name | 1 | 20150828 |
| c6b65c52-69c7-df49-550a-a50c137f6218 | Product name | 1 | 20140508 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 73653-210-01 | Dentemp Canker Cover | 1 in 1 BLISTER PACK | TABLET, EXTENDED RELEASE | 1 | 2 | |
| 73653-210-08 | Dentemp Canker Cover | 8 in 1 CARTON | TABLET, EXTENDED RELEASE | 8 | 2 |
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 |
|---|---|---|---|---|---|---|
| Crest Kids Advanced Color Changing | SODIUM MONOFLUOROPHOSPHATE | Procter & Gamble Manufactura, S de R.L. de C.V. | fc86b98e-d556-4769-e053-6394a90afc6e | 2026-01-08 | Warnings | M022 |
| Care One Maximum Strength | FLUORIDE | American Sales | 1b6618ea-6533-41d7-be2c-13bb9e108dc5 | 2026-01-08 | Warnings | M022 |
| equate Sensitive | POTASSIUM NITRATE, SODIUM FLUORIDE | Wal-Mart Stores Inc | 79899b59-3a16-6504-e053-2991aa0a895a | 2026-01-08 | Warnings | M022 |
| Crest Kids Advanced Color Changing | SODIUM MONOFLUOROPHOSPHATE | Procter & Gamble Manufactura, S de R.L. de C.V. | 451283d3-78b0-8361-e063-6294a90a1fd5 | 2026-01-08 | Warnings | M022 |
| CVS Maximum Strength | BENZOCAINE | CVS Pharmacy | 8691d6b6-741e-47b2-8332-76742b34715f | 2026-01-08 | Warnings | M022 |
| 4x Medicated Toothache and Gum Gel | BENZOCAINE | Publix Super Markets INC | 16eb9d15-dba3-36e6-e063-6394a90ab859 | 2026-01-08 | Warnings | M022 |
| Toothache and Gum Relief | BENZOCAINE, MENTHOL | CVS Pharmacy | 814ec7bf-f825-1095-e053-2a91aa0aee59 | 2026-01-08 | Warnings | M022 |
| Lemon | GLYCERIN | Sion Biotext Medical Ltd | dbd7ed86-1b92-4471-827a-89f3afa1b0dc | 2026-01-08 | Warnings | M022 |
| Sootheez Organic Wild Cherry | PECTIN | BFY LLC | 47baa2a8-270c-fa07-e063-6394a90a97f6 | 2026-01-06 | Warnings | M022 |
| Parodontax Gum Strengthen and Protect | CETYLPYRIDINIUM CHLORIDE | Haleon US Holdings LLC | 3bb378c8-14b2-aa13-e063-6294a90a4db3 | 2026-01-05 | Warnings | M022 |
| MySweetSmile Toothpaste. | MYSWEETSMILE TOOTHPASTE. | Jiangxi Dentalbright Technology Co., Ltd | 478baf87-9276-7288-e063-6294a90a9e8e | 2026-01-04 | Warnings | M022 |
| MySweetSmile Mango Toothpaste. | MYSWEETSMILE MANGO TOOTHPASTE. | Jiangxi Dentalbright Technology Co., Ltd | 478cbdeb-28e1-fa56-e063-6294a90af124 | 2026-01-04 | Warnings | M022 |
| Smile Paint | SODIUM FLUORIDE | JABBER JAW KIDS TOOTHPASTE LLC | a7463b5c-53b2-4353-a5ea-800fbd7bd17d | 2026-01-02 | Warnings | M022 |
| Dentek Canker Cover | MENTHOL | Bershtel Enterprises | 2669183c-7a58-037e-e054-00144ff88e88 | 2025-12-31 | Warnings | M022 |
| AutoBrush strawberry | SODIUM FLUORIDE | Lander Enterprises, LLC | 05929148-bffe-439f-a9d4-3170816c0fa2 | 2025-12-31 | Warnings | M022 |
| AutoBrush Watermelon | SODIUM FLUORIDE | Lander Enterprises, LLC | 37a4e712-e3b5-42f6-971c-98dea4b8dd06 | 2025-12-31 | Warnings | M022 |
| AutoBrush Mint | SODIUM FLUORIDE | Lander Enterprises, LLC | 6bcd35f5-18ea-4fc8-84cd-06db73f38a1e | 2025-12-31 | Warnings | M022 |
| AutoBrush Bubblegum | SODIUM FLUORIDE | Lander Enterprises, LLC | e7bf7e31-650d-4a1c-9100-48722344b201 | 2025-12-31 | Warnings | M022 |
| Normal Salt | SODIUM CHLORIDE | GRAXCELL PHARMACEUTICAL, LLC | f3f09817-8a38-4aa1-956b-69d9cf695074 | 2025-12-25 | Warnings | M022 |
| Sensitive Mint Tooth-paste | POTASSIUM NITRATE, SODIUM FLUORIDE | Meijer, Inc. | 1e5e8b24-8304-482c-ae80-73effcc345da | 2025-12-23 | Warnings | M022 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 2628246 | menthol 2.5 MG Buccal Tablet | PSN | 2e7fbf9d-553c-c7bf-e063-6294a90a5f79 | 2 |
| 2628246 | menthol 2.5 MG Buccal Tablet | SCD | 2e7fbf9d-553c-c7bf-e063-6294a90a5f79 | 2 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 73653-210-01 | 73653021001 | 1 in 1 BLISTER PACK | Historical | ||||
| 73653-210-08 | 73653021008 | 8 BLISTER PACK in 1 CARTON (73653-210-08) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (73653-210-01) | 8 blister pack | 2023-02-02 | No | No | Current |