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 |
|---|---|---|---|---|---|---|
| Sore Mouth Cleanser | HYDROGEN PEROXIDE | Meijer, Inc. | c9c17224-9304-403a-b6a1-9c8bd94e3d94 | 2026-02-19 | Warnings, Adverse reactions | M022 |
| AQUAFRESH CAVITY PROTECTION | SODIUM FLUORIDE | Haleon US Holdings LLC | 5484999c-8e6f-430d-99a5-6893a2489467 | 2026-02-16 | Warnings | M022 |
| AQUAFRESH EXTREME CLEAN WHITENING ACTION | SODIUM FLUORIDE | Haleon US Holdings LLC | aaff19d9-4ba5-462a-893b-7220feb25d6c | 2026-02-16 | Warnings | M022 |
| Oral Sore Antiseptic | HYDROGEN PEROXIDE, MENTHOL | Walgreen Co. | 55807b18-42ed-45a7-845e-fcf7f5d70d04 | 2026-02-12 | Warnings, Adverse reactions | m022 |
| Sore Mouth Cleanser | HYDROGEN PEROXIDE | Walgreen Co. | 33223589-4ff4-4e4e-96da-6fa2e4d0f187 | 2026-02-12 | Warnings, Adverse reactions | M022 |
| PERIOSCIENCES SENSITIVE AO Pro | POTASSIUM NITRATE, SODIUM MONOFLUOROPHOSPHATE | PERIOSCIENCES LLC | acca8964-b575-468c-8b40-514dfbf50778 | 2026-02-09 | Warnings | M022 |
| Oral Sore Antiseptic | HYDROGEN PEROXIDE, MENTHOL | Retail Business Services, LLC | d46546d0-c6df-431a-8ab0-bc5013c084d7 | 2026-02-06 | Warnings, Adverse reactions | M022 |
| Hydrogen Peroxide 3 Percent | HYDROGEN PEROXIDE | EQUATE (Wal-Mart Stores, Inc.) (see also WAL-MART INC) | e19228e9-6f87-456e-a222-f979a234d589 | 2026-02-06 | Warnings | M022 |
| Listerine UltraClean Plus Whitening Protection Intense Antiseptic Antigingivitis/ Antiplaque Mouthwash | EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL | Kenvue Brands LLC | 49d28991-b68f-ba16-e063-6394a90a0b13 | 2026-02-02 | Warnings | M022 |
| Sootheez Strawberry Lemonade | PECTIN | Primrose Candy Co. | 49e2b303-1018-cd13-e063-6394a90ae300 | 2026-02-02 | Warnings | M022 |
| Sootheez Berry Lemonade | PECTIN | Primrose Candy Co. | 49cee56f-c45f-6c79-e063-6294a90a5f8f | 2026-02-01 | Warnings | M022 |
| Sore Mouth Cleanser | HYDROGEN PEROXIDE | Rite Aid Corporation | 294418aa-640d-42be-ad07-de31da7a7ccc | 2026-01-30 | Warnings, Adverse reactions | M022 |
| Ora YoGu 4X Medicated Tooth and Gum Pain Reliever | MEDICATED TOOTH AND GUM PAIN RELIEVER | Kungpo Health Care & Herbal Center Inc | aa61ce6f-8336-4071-93b8-549fd22d1ae0 | 2026-01-22 | Warnings | M022 |
| Colgate Sensitive Complete Protection | POTASSIUM NITRATE AND SODIUM FLUORIDE | Colgate-Palmolive Company | 866067b9-3dce-492d-ae99-1b807ecd56ff | 2026-01-22 | Warnings | M022 |
| Family Wellness Pain Relief | BENZOCAINE 20% | FAMILY DOLLAR (Family Wellness) | 92fa0693-fca5-4bf9-8fce-a2d7e9ca37ea | 2026-01-21 | Warnings | M022 |
| Crest Pro-Health All Day Clean Breath | CETYLPYRIDINIUM CHLORIDE | The Procter & Gamble Manufacturing Company | 48eaca4c-19c2-2dd2-e063-6394a90a3e08 | 2026-01-21 | Warnings | M022 |
| Betadine Gargle | POVIDONE-IODINE | Atlantis Consumer Healthcare, Inc. | 5f0a3377-1398-2603-c632-f0d214bb88ec | 2026-01-21 | Warnings | M022 |
| ORAL PAIN RELIEF | BENZOCAINE | Universal Distribution Center LLC | e276ba37-46fb-4ed9-9ee1-c08a2a89704a | 2026-01-20 | Warnings | M022 |
| Equate Orasol | 20% BENZOCAINE | WAL-MART STORES INC. | 08404780-8252-4484-b1c3-8970803f74f8 | 2026-01-19 | Warnings | M022 |
| Equate Healthy Mouth | CPC 0.05% ANTIPLAQUE/ANTI-GINGIVITIS | Walmart, Inc. | 1cc1f6fd-67d4-b314-e063-6294a90ab995 | 2026-01-19 | 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 |