NDC 0283-1016-00 - HurriCaine 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
- 0283-1016
- Requested NDC
- 0283-1016-00
- Package NDCs from labels
- 0283-1016-00, 0283-1016-31, 0283-1016-43, 0283-1016-45, 0283-1016-59
- Manufacturer
- Beutlich Pharmaceuticals, LLC | Dental Technologies | Speciality Pharma Manufacturing
- Effective date
- 2025-01-08
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| SB Gel | Beutlich Pharmaceuticals, LLC | Dental Technologies | Speciality Pharma Manufacturing | 2025-01-08 | HUMAN OTC DRUG LABEL |
| BENZOCAINE - Beutlich Pharmaceuticals, LLC | Centrix Inc. | Dental Technologies | Beutlich Pharmaceuticals, LLC | Centrix Inc. | Dental Technologies | 2024-10-28 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0283-1016-00 | HurriCaineTopical Anesthetic | 28.4 g in 1 BOTTLE, PLASTIC | GEL | 28.4 | 45 | |
| 0283-1016-31 | HurriCaineTopical Anesthetic | 1 in 1 BOX | GEL | 1 | 45 | |
| 0283-1016-43 | HurriCaineTopical Anesthetic | 1 g in 1 PACKET | GEL | 1 | 45 | |
| 0283-1016-45 | HurriCaineTopical Anesthetic | 0.5 g in 1 CUP, UNIT-DOSE | GEL | 0.5 | 6 | |
| 0283-1016-59 | HurriCaineTopical Anesthetic | 60 in 1 BOX | GEL | 60 | 6 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 0283-1016 | HURRICAINE TOPICAL ANESTHETIC (BENZOCAINE) GEL [BEUTLICH PHARMACEUTICALS, LLC] | 45 | Current NDC, Legacy NDC, 3 package rows | 20250110_42521b29-67e4-4a16-848d-7e6ba4a7ece2.zip |
| 0283-1016 | HURRICAINE TOPICAL ANESTHETIC (BENZOCAINE) GEL [BEUTLICH PHARMACEUTICALS, LLC] | 6 | Current NDC, Legacy NDC, 2 package rows | 20241030_0605d5d6-82bd-415e-b5cb-e273f934a4a7.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0283-1016-31 | GM - Gram | 0283-1016 | 63b9ec1c-583b-4b8e-bdc3-b8b655959561 | 1 | 2018-05-09 |
| 0283-1016-45 | EA - Each | 0283-1016 | 8385d8b9-ec94-4266-84a9-7b44ed56fa24 | 1 | 2022-03-09 |
| 0283-1016-59 | EA - Each | 0283-1016 | 8952eeef-e587-474c-98cf-a7386719c335 | 1 | 2022-03-09 |
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 |
|---|---|---|---|---|---|---|
| CrystLCare Regeneration Plus | POTASSIUM NITRATE, SODIUM FLUORIDE | GreenMark Biomedical Inc. | 4f86d0a0-d73e-5605-e063-6394a90adb38 | 2026-09-14 | Warnings | M022 |
| Opalescence Whitening Sensitivity Relief | POTASSIUM NITRATE AND SODIUM FLUORIDE | Ultradent Products, Inc. | 44e94663-895b-67da-e063-6394a90a5fe6 | 2026-09-09 | Warnings | M022 |
| Opalescence Sensitivity Relief Whitening | POTASSIUM NITRATE AND SODIUM FLUORIDE | Ultradent Products, Inc. | b5176a84-76a3-4ad0-a2e2-4997a12da9a5 | 2026-09-09 | Warnings | M022 |
| Opal by Opalescence Sensitivity | POTASSIUM NITRATE AND SODIUM FLUORIDE | Ultradent Products, Inc. | 5ffc0d14-0290-47bb-90e5-90a25a5acc28 | 2026-09-09 | Warnings | M022 |
| Saline | NASAL | Raritan Pharmaceuiticals Inc | 4b178e4e-a10f-4b75-8140-1f7548e203ad | 2026-09-09 | Warnings | M022 |
| SORE THROAT | PHENOL | Raritan Pharmaceuticals Inc | 43ce374a-824c-4034-bf04-c351b4d8015b | 2026-09-08 | Warnings | M022 |
| Colgate Optic White Stain Fighter Sens Relief | SODIUM FLUORIDE | Colgate-Palmolive Company | 6ec2fff7-df44-4302-be2d-97946c6cd66a | 2026-09-08 | Warnings | M022 |
| DRx Choice Sore Throat Menthol Flavor | PHENOL | RARITAN PHARMACEUTICALS INC | e3269b12-5c05-45a6-81f2-65d9f016c3aa | 2026-09-08 | Warnings | M022 |
| Sting Relief Pad | BENZOCAINE, ISOPROPYL ALCOHOL CLOTH | JINHUA JINGDI MEDICAL SUPPLIES CO., LTD | 57ccc28b-5f5f-30ec-e063-6294a90a081c | 2026-09-07 | Warnings | U3RSY48JW5 |
| Dr.Harry EYES PROTECTION | POLYETHYLENE GLYCOL 400 1% EYES PROTECTION | Wenzhou Yuyuan Pharmaceutical Co., Ltd. | 5a9fe033-89d3-da62-e063-6294a90a4503 | 2026-09-03 | Warnings | B697894SGQ |
| SurviveX Sting Relief | STING RELIEF WIPE | Changzhou Maokang Medical Products Co., Ltd. | 5a83b1f1-c8dc-cf07-e063-6394a90a20ca | 2026-09-03 | Warnings | U3RSY48JW5 |
| Hydrogen Peroxide | HYDROGEN PEROXIDE | AmerisourceBergen (Good Neighbor Pharmacy) 46122 | 0733015b-e81a-4a62-82ad-dacaf3f163cb | 2026-09-02 | Warnings | M022 |
| KROGER Saline | NASAL | KROGER COMPANY | c84b242b-f46e-4ea8-a3c1-109a47644646 | 2026-09-02 | Warnings | M022 |
| Antiseptic | EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL | WALMART INC. (see also Equate) | ceb125d9-8c1b-498c-b0f0-f18756ede442 | 2026-09-01 | Warnings | M022 |
| Orajel 4X Medicated Toothache and Gum Cream | BENZALKONIUM CHLORIDE, BENZOCAINE, MENTHOL, ZINC CHLORIDE | Church & Dwight Co., Inc. | 5a1c82b4-02b3-d456-e063-6294a90a16bb | 2026-08-31 | Warnings | M022 U3RSY48JW5 |
| Orajel 4X Medicated Toothache and Gum PM Cream | BENZALKONIUM CHLORIDE, BENZOCAINE, MENTHOL, ZINC CHLORIDE | Church & Dwight Co., Inc. | 5a1cdaf4-3388-280c-e063-6294a90ac70f | 2026-08-31 | Warnings | M022 U3RSY48JW5 |
| MUCINEX INSTASOOTHE SORE THROAT PLUS SOOTHING COMFORT | HEXYLRESORCINOL | Reckitt Benckiser LLC | 91cd2964-5d83-4e40-bc18-e3e5462f454a | 2026-08-31 | Warnings | M022 |
| MUCINEX INSTASOOTHE SORE THROAT PLUS PAIN RELIEF | HEXYLRESORCINOL | Reckitt Benckiser LLC | 4c150222-06ea-4fcf-967f-84e19846bd66 | 2026-08-31 | Warnings | M022 |
| Orajel 4X Medicated Toothache and Gum | BENZALKONIUM CHLORIDE, BENZOCAINE, MENTHOL, ZINC CHLORIDE | Church & Dwight Co., Inc. | 5a1b4133-0eac-2f8f-e063-6394a90af8f6 | 2026-08-28 | Warnings | M022 U3RSY48JW5 |
| LUDENS SUGAR FREE WILD CHERRY THROAT | PECTIN | Prestige Brands Holdings, Inc. | 274fc80c-e5b2-41c7-a119-287d6e8a2258 | 2026-08-28 | Warnings | M022 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.