NDC 51206-202
UltraCare Oral Anesthetic Walterberry
Benzocaine
UltraCare Oral Anesthetic Walterberry is a Dental Gel in the Human Otc Drug category. It is labeled and distributed by Ultradent Products, Inc.. The primary component is Benzocaine.
| Product ID | 51206-202_19052b2e-209d-4151-a35c-2ee002fb4fdb |
| NDC | 51206-202 |
| Product Type | Human Otc Drug |
| Proprietary Name | UltraCare Oral Anesthetic Walterberry |
| Generic Name | Benzocaine |
| Dosage Form | Gel |
| Route of Administration | DENTAL |
| Marketing Start Date | 1993-06-01 |
| Marketing End Date | 2024-12-31 |
| Marketing Category | OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL |
| Application Number | part356 |
| Labeler Name | Ultradent Products, Inc. |
| Substance Name | BENZOCAINE |
| Active Ingredient Strength | 200 mg/mL |
| NDC Exclude Flag | N |
Packaging
NDC 51206-202-01
30 mL in 1 BOTTLE (51206-202-01)
| Marketing Start Date | 1993-06-01 |
| Marketing End Date | 2023-01-08 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 51206-202-02 [51206020202]
UltraCare Oral Anesthetic Walterberry GEL
| Marketing Category | OTC MONOGRAPH NOT FINAL |
| Application Number | part356 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 1993-06-01 |
| Marketing End Date | 2023-12-31 |
NDC 51206-202-05 [51206020205]
UltraCare Oral Anesthetic Walterberry GEL
| Marketing Category | OTC MONOGRAPH NOT FINAL |
| Application Number | part356 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 1993-06-01 |
| Marketing End Date | 2023-12-31 |
NDC 51206-202-03 [51206020203]
UltraCare Oral Anesthetic Walterberry GEL
| Marketing Category | OTC MONOGRAPH NOT FINAL |
| Application Number | part356 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 1993-06-01 |
| Marketing End Date | 2023-12-31 |
NDC 51206-202-04 [51206020204]
UltraCare Oral Anesthetic Walterberry GEL
| Marketing Category | OTC MONOGRAPH NOT FINAL |
| Application Number | part356 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 1993-06-01 |
| Marketing End Date | 2023-07-31 |
NDC 51206-202-01 [51206020201]
UltraCare Oral Anesthetic Walterberry GEL
| Marketing Category | OTC MONOGRAPH NOT FINAL |
| Application Number | part356 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 1993-06-01 |
Drug Details
Active Ingredients
| Ingredient | Strength |
|---|---|
| BENZOCAINE | 200 mg/mL |
OpenFDA Data
| SPL SET ID: | 87317d3c-ddda-403a-ad61-e2da9d50356a |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
NDC Crossover Matching brand name "UltraCare Oral Anesthetic Walterberry" or generic name "Benzocaine"
| NDC | Brand Name | Generic Name |
|---|---|---|
| 51206-202 | UltraCare Oral Anesthetic Walterberry | UltraCare Oral Anesthetic Walterberry |
| 0283-0220 | HurriCaine | Benzocaine |
| 0283-0293 | HurriCaine | Benzocaine |
| 0283-0520 | HurriCaine | Benzocaine |
| 0283-0569 | HurriCaine | Benzocaine |
| 0283-0679 | HurriCaine | Benzocaine |
| 0283-0871 | HurriCaine | BENZOCAINE |
| 0283-0886 | HurriCaine | Benzocaine |
| 0283-0914 | HurriCaine | Benzocaine |
| 0283-0920 | HurriCaine | Benzocaine |
| 0283-0998 | HurriCaine | Benzocaine |
| 0283-1016 | HurriCaine | BENZOCAINE |
Trademark Results [UltraCare]
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