NDC 76357-491 - SmartMouth Mouth Sore Zinc Activated Formula
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 76357-491
- Manufacturer
- Triumph Pharmaceuticals Inc.
- Effective date
- 2023-12-21
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| SmartMouth Mouth Sore Solution 1 - Triumph Pharmaceuticals Inc. | Triumph Pharmaceuticals Inc. | 2023-12-21 | HUMAN OTC DRUG LABEL |
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 |
|---|---|---|---|---|---|---|
| Dr. Blue | MENTHOL | Indiana Botanic Gardens | 1b1150bd-e087-4d8f-b0d6-0d935cf6e31e | 2016-11-01 | Warnings | L7T10EIP3A |
| Professional Therapy MuscleCare | CAMPHOR, MENTHOL | Active and Innovative Inc. | 1ec95bbb-cd7d-2588-e054-00144ff8d46c | 2016-08-11 | Warnings | L7T10EIP3A |
| Professional Therapy MuscleCare pain relieving gel Extra Strength | CAMPHOR, MENTHOL | Active and Innovative Inc. | 1d2403d9-99c3-24f5-e054-00144ff8d46c | 2016-08-10 | Warnings | L7T10EIP3A |
| MED AID CHEST RUB | MENTHOL AND CAMPHOR AND EUCALYPTUS OIL | Blue Cross Laboratories, Inc. | 429041fe-55a5-4df1-b60d-721103e5c65e | 2016-07-27 | Warnings | L7T10EIP3A |
| Sterile Water | WATER | Baxter Healthcare Company | 210dc9ab-d6ca-4552-ac19-1be17792d290 | 2016-05-31 | Warnings, Adverse reactions | 059QF0KO0R |
| Eagle Brand Medicated Roll On Refresh | CAMPHOR, MENTHOL | Borden Company (Private) Limited | 567b6820-fb52-630e-e063-6294a90a8bf8 | 2015-07-01 | Warnings | AV092KU4JH |
| Eagle Brand Medicated Oil Aromatic | CAMPHOR, MENTHOL, METHYL SALICYLATE | Borden Company (Private) Limited | 54e45d89-e8c3-6fc3-e063-6394a90aac4e | 2015-06-15 | Warnings | L7T10EIP3A |
| Sodium Chloride | SODIUM CHLORIDE | Baxter Healthcare Corporation | 2a96096d-43cc-49b7-af53-b53c17f41001 | 2014-07-25 | Warnings, Adverse reactions | 451W47IQ8X |
| SODIUM CHLORIDE | SODIUM CHLORIDE | Baxter Healthcare Corporation | b3b4b176-41f0-4ca8-90d4-3fba5707564a | 2014-02-21 | 451W47IQ8X | |
| TIS-U-SOL | SODIUM CHLORIDE, POTASSIUM CHLORIDE, MAGNESIUM SULFATE, SODIUM PHOSPHATE, AND POTASSIUM PHOSPHATE | Baxter Healthcare Corporation | 9da4121f-d62d-4da4-8dfb-0494da16015f | 2014-02-21 | 451W47IQ8X | |
| Ringers | SODIUM CHLORIDE, CALCIUM CHLORIDE, POTASSIUM CHLORIDE, | Baxter Healthcare Corporation | e1953d54-818d-46a6-8532-518ebae6d84e | 2012-06-13 | 451W47IQ8X | |
| Lactated Ringers | SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE | Baxter Healthcare Corporation | f09f80bf-2f8b-4420-865d-aec2d5e5cd4d | 2012-06-12 | 451W47IQ8X |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.