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 |
|---|---|---|---|---|---|---|
| GingiCaine Gel, Mint Julep | GINGICAINE GEL, MINT JULEP FLABVOR | Gingi-Pak a Division of the Belport | 6285fe10-08ba-8044-e053-2991aa0a8e8b | 2026-06-29 | Warnings | M022 |
| GingiCaine Gel, Pina Colada | GINGICAINE GEL, PINA COLADA FLAVOR | Gingi-Pak a Division of the Belport | 6284e1fe-be33-69bf-e053-2991aa0a90ab | 2026-06-29 | Warnings | M022 |
| GingiCaine Gel, Chocolate Mint | GINGICAINE GEL, CHOCOLATE MINT FLAVOR | Gingi-Pak a Division of the Belport | 6285c4f2-c139-49a9-e053-2991aa0a2b03 | 2026-06-29 | Warnings | M022 |
| UltraCare Anesthetic Gel | BENZOCAINE | The Bellport Company, Inc. dba Gingi-Pak | f5dd8fa8-0b6a-5a30-e053-2995a90ad194 | 2026-06-26 | Warnings | M022 |
| GingiCaine Gel | GINGICAINE GEL BANANA FLAVOR | Gingi-Pak a Division of the Belport | 62857d06-a829-4efa-e053-2991aa0a6d15 | 2026-06-25 | Warnings | M022 |
| GingiCaine Gel, Cotton Candy Flavor | GINGICAINE GEL, COTTON CANDY FLAVOR | Gingi-Pak a Division of the Belport | 628515a5-175f-ac2c-e053-2991aa0a19ce | 2026-06-25 | Warnings | M022 |
| Perox-A-Mint Solution | HYDROGEN PEROXIDE | Sage Products, LLC | 50823ff5-ad08-4449-bc4a-9a8ae25ec0d5 | 2026-06-24 | Warnings | M022 |
| Antiseptic Oral Rinse | CETYLPYRIDINIUM CHLORIDE | Sage Products LLC | efff8bae-154d-46bc-8dd4-716800425663 | 2026-06-24 | M022 | |
| Anbesol Maximum Strength | BENZOCAINE | Foundation Consumer Brands | 8c6ac499-9bd2-4ea5-9f26-df7947bff4a6 | 2026-06-22 | Warnings | M022 |
| Anbesol Maximum Strength | BENZOCAINE | Foundation Consumer Brands | dcc37403-0192-4658-bb7a-059273ce0047 | 2026-06-22 | Warnings | M022 |
| Toothache | POLYHEXAMETHYLENE BIGUANIDE HYDROCHLORIDE | Guchutang Biotechnology (Longyan) Co., Ltd | 54ad2ceb-272f-e5ba-e063-6394a90aec5f | 2026-06-20 | Warnings | M022 |
| Hydrogen Peroxide | HYDROGEN PEROXIDE | Delon Laboratories (1990) Ltd | d4aa09bf-8207-47dd-bc42-01e660da9438 | 2026-06-16 | Warnings | M022 |
| TideFresh MOUTH SORE AND TOOTHACHE | BENZOCAINE 20% MOUTH SORE AND TOOTHACHE | Wenzhou Yuyuan Pharmaceutical Co., Ltd. | 541e1814-c00e-efdf-e063-6394a90a41a1 | 2026-06-13 | Warnings | M022 |
| Chloraseptic Sore Throat Max | PHENOL AND GLYCERIN | Prestige Brands Holdings, Inc. | 882c940c-b3c3-4aa4-8d64-e4260f066ff4 | 2026-06-08 | Warnings | M022 |
| Orazen | SODIUM MONOFLUOROPHOSPHATE | Orazen Inc | fa5b6bd8-443f-79e7-e053-6394a90a5513 | 2026-06-03 | Warnings | M022 |
| Fishermans Friend Mixed Berry | MENTHOL | Lofthouse of Fleetwood | 53391c4d-ee2d-ade3-e063-6394a90ac77d | 2026-06-01 | Warnings | M022 |
| Orajel Medicated for Toothache and Gum, Liquid | BENZOCAINE AND MENTHOL | Church & Dwight Co., Inc. | ac3d605d-241d-1a6f-e053-2a95a90ae391 | 2026-06-01 | Warnings | M022 |
| MUCINEX INSTASOOTHE SORE THROAT PLUS PAIN RELIEF | BENZOCAINE AND MENTHOL, UNSPECIFIED FORM | Reckitt Benckiser LLC | 6140d487-d87c-4954-9247-83492bcc5738 | 2026-05-27 | Warnings | M022 |
| Dolodent Maximum Strength | BENZOCAINE | Pharmadel LLC | 351ecc2b-cc1a-2bbf-e063-6394a90a5c14 | 2026-05-26 | Warnings | M022 |
| MOUTH ULCER | PANTHENOL | Guangzhou Shengli Shidai Cosmetics Co., Ltd. | 5264f81c-bffe-4f6d-e063-6394a90ae3bf | 2026-05-22 | 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 |