Maximum Strength Cold Sore Treatment
- Product NDC
- 41250-411
- 11-digit product format
- 412500411
- Labeler code
- 41250
- Product ID
- 41250-411_ed54cd45-c7cf-4437-8773-95c4c3d37390
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Camphor, Menthol, Phenol, White Petrolatum
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Meijer Distribution Inc
- Application
- M022
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2019-09-09
- Substance
- CAMPHOR (SYNTHETIC); MENTHOL, UNSPECIFIED FORM; PHENOL; PETROLATUM
- Active strength
- 30; 10; 15; 892 mg/g; mg/g; mg/g; 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
- Maximum Strength Cold Sore Treatment
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| CAMPHOR (SYNTHETIC) | 30 mg/g |
| MENTHOL, UNSPECIFIED FORM | 10 mg/g |
| PHENOL | 15 mg/g |
| PETROLATUM | 892 mg/g |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| 5TJD82A1ET | Internal UNII lookup |
| L7T10EIP3A | Internal UNII lookup |
| 339NCG44TV | Internal UNII lookup |
| 4T6H12BN9U | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 2175793 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 9220772c-b3b7-4855-e053-2a95a90a94f6 | Available on FDA.report |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 41250-411-01 | 2021-02-17 | C162847 | 48780-1 | ba0f9c33-3f6c-a910-e053-dadaa90a0b85 | Maximum Strength Cold Sore Treatment - Meijer |
| 41250-411-01 | 2021-01-29 | C162847 | 48780-1 | ba0f9c33-3f6c-a910-e053-dadaa90a0b85 | Maximum Strength Cold Sore Treatment - Meijer |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 41250-411-01 | Maximum Strength Cold Sore Treatment | 2 g in 1 TUBE | GEL | 2 | 6 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 41250-411 | MAXIMUM STRENGTH COLD SORE TREATMENT (CAMPHOR, MENTHOL, PHENOL, WHITE PETROLATUM) GEL [MEIJER DISTRIBUTION INC] | 6 | Current NDC, Legacy NDC, 1 package rows | 20241128_9220772c-b3b7-4855-e053-2a95a90a94f6.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 |
|---|---|---|---|---|---|---|
| SENSODYNE Rapid Relief | STANNOUS FLUORIDE | Haleon US Holdings LLC | f9589e7c-c5ca-4465-8d37-47ad6c69249f | 2024-03-06 | Warnings | M022 |
| SENSODYNE Repair and Protect Extra Fresh | STANNOUS FLUORIDE | Haleon US Holdings LLC | 34260c69-d829-46c0-b12a-5136ee073ba1 | 2024-03-06 | Warnings | M022 |
| AQUAFRESH SENSITIVE MAXIMUM STRENGTH | POTASSIUM NITRATE AND SODIUM FLUORIDE | Haleon US Holdings LLC | 76adbccb-0812-4407-a6fc-a57e6f144fbb | 2024-03-05 | Warnings | M022 |
| SENSODYNE Advanced Whitening | POTASSIUM NITRATE | Haleon US Holdings LLC | a06e2549-3c4e-4818-b53e-1dea6828219f | 2024-03-04 | Warnings | M022 |
| Sensodyne Extra Whitening Cool Mint | POTASSIUM NITRATE AND SODIUM FLUORIDE | Haleon US Holdings LLC | c977f2c4-e0f3-44d2-aa7a-845f0583af3e | 2024-03-04 | Warnings | M022 |
| Sensodyne Natural white | POTASSIUM NITRATE AND SODIUM FLUORIDE | Haleon US Holdings LLC | 911ac7e4-2b92-43d5-af0b-b5f741b088fb | 2024-03-04 | Warnings | M022 |
| Sensodyne Nourish Healthy White | POTASSIUM NITRATE AND SODIUM FLUORIDE | Haleon US Holdings LLC | aca38560-2fd7-47be-9e93-2abc3214e856 | 2024-03-04 | Warnings | M022 |
| Sensodyne Nourish Gently Soothing | POTASSIUM NITRATE AND SODIUM FLUORIDE | Haleon US Holdings LLC | 5403ab67-532c-4bdf-9b06-07b1866f37f1 | 2024-03-04 | Warnings | M022 |
| SENSODYNE PRONAMEL Active Shield Fresh Mint | POTASSIUM NITRATE AND SODIUM FLUORIDE | Haleon US Holdings LLC | e8684615-f544-4871-b935-0a0f93639d7d | 2024-03-04 | Warnings | M022 |
| Sensodyne Pronamel Gentle Whitening Fresh Mint | POTASSIUM NITRATE AND SODIUM FLUORIDE | Haleon US Holdings LLC | 3dfa6827-3aae-4f19-93f6-2ded2faf2ddd | 2024-03-04 | Warnings | M022 |
| Made by Dentists Sensitive and Whitening Fresh Mint | POTASSIUM NITRATE, SODIUM FLUORIDE | MADE BY DENTISTS INC | 0d379c26-69ff-4666-9ad5-7618f0bd139f | 2024-02-27 | Warnings | M022 |
| Polident ProPartial | STANNOUS FLUORIDE | Haleon US Holdings LLC | 557eeb32-64f4-41e8-ada4-91bd39ae2920 | 2024-02-07 | Warnings | M022 |
| SENSODYNE PRONAMEL Daily Protection | POTASSIUM NITRATE AND SODIUM FLUORIDE | Haleon US Holdings LLC | edffce4d-108b-4ffd-9adf-e12cb42ffddd | 2024-01-24 | Warnings | M022 |
| Peppermint Twist | FLUORIDE | Caldwell Health LLC | 4b28cdd1-0dba-42f5-a9e8-06d9e75b2396 | 2024-01-17 | Warnings | M022 |
| The Natural Dentist Groovy Grape | FLUORIDE | Caldwell Consumer Health LLC | 087abbed-1f58-4b45-a76b-a950fa81c18c | 2024-01-16 | Warnings | M022 |
| Benzoin Tincture | BENZOIN RESIN | Pharma Nobis, LLC | e42fccc2-1b4f-e7f3-e053-2a95a90aef39 | 2023-12-26 | Warnings | M022 |
| Sunmark Benzoin Compound Tincture | BENZOIN RESIN | Strategic Sourcing Services LLC | 0c96d810-83dc-47d3-9a75-63a79feaad0a | 2023-12-19 | Warnings | M022 |
| Benzoin Tincture | BENZOIN RESIN | Humco Holding Group, Inc. | b33b5896-673b-498c-8a58-76ece8552f7a | 2023-12-15 | Warnings | M022 |
| Povidone Iodine | POVIDONE IODINE ORAL RINSE 0.5% | Humco Holding Group, Inc. | b83dbdd1-ff63-caf8-e053-2a95a90a5764 | 2023-12-15 | Warnings | M022 |
| Moon Whitening Gel Anticavity | SODIUM FLUORIDE | Moon Oral Care, LLC | 0c556a29-a697-3a66-e063-6394a90abfee | 2023-12-12 | Warnings | M022 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 2175793 | camphor 3 % / menthol 1 % / petrolatum 89.2 % / phenol 1.5 % Topical Gel | PSN | 9220772c-b3b7-4855-e053-2a95a90a94f6 | 6 |
| 2175793 | camphor 0.03 MG/MG / menthol 0.01 MG/MG / petrolatum 0.892 MG/MG / phenol 0.015 MG/MG Topical Gel | SCD | 9220772c-b3b7-4855-e053-2a95a90a94f6 | 6 |
| 2175793 | camphor 3 % / menthol 1 % / petrolatum 89.2 % / phenol 1.5 % Topical Gel | SY | 9220772c-b3b7-4855-e053-2a95a90a94f6 | 6 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 41250-411-01 | 41250041101 | 2 g in 1 TUBE (41250-411-01) | 2 g | 2019-09-09 | 0000-00-00 | No | No | Current |