NDC 55346-2902-01 - Alpha-Caine Topical Anesthetic
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
- 55346-2902
- Requested NDC
- 55346-2902-01
- Package NDCs from labels
- 55346-2902-1, 55346-2902-01
- Manufacturer
- Dental Technologies, Inc.
- Effective date
- 2025-11-04
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Alpha-Caine Drug Facts, Mint | Dental Technologies, Inc. | 2025-11-04 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 55346-2902-1 | Alpha-CaineTopical Anesthetic | 30 g in 1 BOTTLE, PLASTIC | GEL | 30 | 9 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 55346-2902 | ALPHA-CAINE TOPICAL ANESTHETIC (BENZOCAINE) GEL [DENTAL TECHNOLOGIES, INC.] | 8 | Current NDC, Legacy NDC, 1 package rows | 20231216_ae628766-25b7-4b4f-abb8-a43faf2f44b9.zip |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| Benzocaine | ACTIVE INGREDIENT | U3RSY48JW5 | ALPHA-CAINE TOPICAL ANESTHETIC (BENZOCAINE) GEL [DENTAL TECHNOLOGIES, INC.] | 5 | |
| Benzocaine | ACTIVE MOIETY | U3RSY48JW5 | ALPHA-CAINE TOPICAL ANESTHETIC (BENZOCAINE) GEL [DENTAL TECHNOLOGIES, INC.] | 5 | |
| D&C YELLOW NO. 10 | INACTIVE INGREDIENT | 35SW5USQ3G | ALPHA-CAINE TOPICAL ANESTHETIC (BENZOCAINE) GEL [DENTAL TECHNOLOGIES, INC.] | 5 | |
| FD&C BLUE NO. 1 | INACTIVE INGREDIENT | H3R47K3TBD | ALPHA-CAINE TOPICAL ANESTHETIC (BENZOCAINE) GEL [DENTAL TECHNOLOGIES, INC.] | 5 | |
| Polyethylene Glycol 3350 | INACTIVE INGREDIENT | G2M7P15E5P | ALPHA-CAINE TOPICAL ANESTHETIC (BENZOCAINE) GEL [DENTAL TECHNOLOGIES, INC.] | 5 | |
| Polyethylene Glycol 400 | INACTIVE INGREDIENT | B697894SGQ | ALPHA-CAINE TOPICAL ANESTHETIC (BENZOCAINE) GEL [DENTAL TECHNOLOGIES, INC.] | 5 | |
| SACCHARIN SODIUM | INACTIVE INGREDIENT | SB8ZUX40TY | ALPHA-CAINE TOPICAL ANESTHETIC (BENZOCAINE) GEL [DENTAL TECHNOLOGIES, INC.] | 5 |
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 |
|---|---|---|---|---|---|---|
| Coleman Sting and Bite Relief | EXTERNAL ANALGESIC AND FIRST AID ANTISEPTIC | Wisconsin Pharmacal Company | 4f94ab35-3099-716c-e063-6294a90a8bea | 2026-04-16 | Warnings | U3RSY48JW5 |
| PEG 3350 and Electrolytes | POLYETHYLENE GLYCOL 3350, SODIUM SULFATE ANHYDROUS, SODIUM BICARBONATE, SODIUM CHLORIDE, POTASSIUM CHLORIDE | Wilshire Pharmaceuticals, Inc. | b251752d-7750-482a-9364-0acf4ad47cc8 | 2026-04-16 | Warnings, Adverse reactions | G2M7P15E5P |
| BiteMD | INSECT BITE RELIEF | Wisconsin Pharmacal Company | 4f860c1e-a638-4923-e063-6294a90ae7e2 | 2026-04-15 | Warnings | U3RSY48JW5 |
| Osstem S Sensitivity relief tooth | POTASSIUM NITRATE, SODIUM FLUORIDE | Osstem Pharma Co., Ltd | 4f8ab179-8f29-a7cf-e063-6294a90a0c22 | 2026-04-15 | Warnings | M022 |
| GoLYTELY | POLYETHYLENE GLYCOL 3350, SODIUM SULFATE ANHYDROUS, SODIUM BICARBONATE, SODIUM CHLORIDE, POTASSIUM CHLORIDE | Azurity Pharmaceuticals, Inc. | 7609ecf7-0ce0-4fbb-9c27-30987f689575 | 2026-04-15 | Warnings, Adverse reactions | G2M7P15E5P |
| TRILYTE | POLYETHYLENE GLYOCOL 3350, SODIUM CHLORIDE, SODIUM BICARBONATE AND POTASSIUM CHLORIDE | Aurobindo Pharma Limited | 79f5e596-8d51-4227-afcc-f5e341150957 | 2026-04-15 | Warnings, Adverse reactions | G2M7P15E5P |
| PEG 3350, sodium chloride, sodium bicarbonate and potassium chloride | POLYETHYLENE GLYCOL 3350, SODIUM CHLORIDE, SODIUM BICARBONATE, POTASSIUM CHLORIDE | Wilshire Pharmaceuticals, Inc. | 4e442a72-b13b-4869-8a1d-59356095b091 | 2026-04-14 | Warnings, Adverse reactions | G2M7P15E5P |
| Crest Pro-Health Gum DetoxifyWinter Mint | CETYLPYRIDINIUM CHLORIDE | The Procter & Gamble Manufacturing Company | 4f6db58f-0b09-d155-e063-6394a90ae658 | 2026-04-14 | Warnings | M022 |
| Lolleez Orange Mango | PECTIN | BFY LLC | 4f6dec8b-078a-f321-e063-6294a90a248c | 2026-04-14 | Warnings | M022 |
| Crest Pro-Health Gum Restore Smooth Mint | CETYLPYRIDINIUM CHLORIDE | The Procter & Gamble Manufacturing Company | 4f6e3b36-e565-7d27-e063-6294a90ae5ac | 2026-04-14 | Warnings | M022 |
| Crest Pro-Health Nightly Bacteria Shield | CETYLPYRIDINIUM CHLORIDE | The Procter & Gamble Manufacturing Company | 4f6ec1e0-c6b5-226f-e063-6294a90a8f14 | 2026-04-14 | Warnings | M022 |
| Sting Relief Swab | BENZOCAINE | 4 Visions LLC | 4f76a8c5-fde6-eee0-e063-6394a90a09f8 | 2026-04-14 | Warnings | U3RSY48JW5 |
| AHLO PRO Healthy Gums | CETYLPYRIDINIUM CHLORIDE | Gervest USA Inc | 4f5a0ccb-26e5-ebb6-e063-6394a90abbc5 | 2026-04-13 | Warnings | M022 |
| Retaine Ultra PF | POLYETHYLENE GLYCOL | OCuSOFT LLC | a5aaaf06-772d-44d3-8601-f978ddc48ad7 | 2026-04-13 | Warnings | B697894SGQ |
| clear lax | POLYETHYLENE GLYCOL 3350 | Meijer Distribution Inc | 6464f12c-0883-46c5-943b-a84fe235588e | 2026-04-13 | Warnings | G2M7P15E5P |
| Crest Scope Original Clean Mint | CETYLPYRIDINIUM CHLORIDE | The Procter & Gamble Manufacturing Company | 4f1db6f4-acd7-a665-e063-6294a90a826b | 2026-04-10 | Warnings | M022 |
| Sore Throat | PHENOL GLYCERIN | Walgreens | 1e845299-178e-49ce-9d08-7e9d548a5a6d | 2026-04-09 | Warnings | M022 |
| Sore throat cherry | PHENOL | Walgreens | 67bed85e-e1e2-49ba-98d6-dfd4e1cd6856 | 2026-04-08 | Warnings | M022 |
| Health-Tec Topical Anesthetic | BENZOCAINE | Dental Health Products, Inc. | 5eb437c5-a2af-4c0d-b7b9-9ab7d093db85 | 2026-04-06 | Warnings | M022 238910 U3RSY48JW5 |
| Antiseptic | EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL | Family Dollar (FAMILY WELLNESS) | 269b9e7f-c5c8-4023-a3ea-e39040ade271 | 2026-04-06 | Warnings | M022 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.