NDC 36987-1742
Spearmint
Spearmint
Spearmint is a Intradermal; Subcutaneous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Nelco Laboratories, Inc.. The primary component is Spearmint.
| Product ID | 36987-1742_dec580ea-73db-4658-9de1-440c19bb42b7 |
| NDC | 36987-1742 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Spearmint |
| Generic Name | Spearmint |
| Dosage Form | Injection, Solution |
| Route of Administration | INTRADERMAL; SUBCUTANEOUS |
| Marketing Start Date | 1972-08-29 |
| Marketing Category | BLA / BLA |
| Application Number | BLA102192 |
| Labeler Name | Nelco Laboratories, Inc. |
| Substance Name | SPEARMINT |
| Active Ingredient Strength | 0 g/mL |
| Pharm Classes | Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Food Additives [CS],Allergens [CS],Dietary Proteins [CS] |
| NDC Exclude Flag | E |
| Listing Certified Through | 2017-12-31 |
Packaging
NDC 36987-1742-2
10 mL in 1 VIAL, MULTI-DOSE (36987-1742-2)
| Marketing Start Date | 1972-08-29 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 36987-1742-3 [36987174203]
Spearmint INJECTION, SOLUTION
| Marketing Category | BLA |
| Application Number | BLA102192 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1972-08-29 |
| Inactivation Date | 2019-10-21 |
NDC 36987-1742-1 [36987174201]
Spearmint INJECTION, SOLUTION
| Marketing Category | BLA |
| Application Number | BLA102192 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1972-08-29 |
| Inactivation Date | 2019-10-21 |
NDC 36987-1742-4 [36987174204]
Spearmint INJECTION, SOLUTION
| Marketing Category | BLA |
| Application Number | BLA102192 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1972-08-29 |
| Inactivation Date | 2019-10-21 |
NDC 36987-1742-2 [36987174202]
Spearmint INJECTION, SOLUTION
| Marketing Category | BLA |
| Application Number | BLA102192 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1972-08-29 |
| Inactivation Date | 2019-10-21 |
Drug Details
Active Ingredients
| Ingredient | Strength |
|---|---|
| SPEARMINT | .05 g/mL |
OpenFDA Data
Pharmacological Class
- Non-Standardized Food Allergenic Extract [EPC]
- Increased Histamine Release [PE]
- Cell-mediated Immunity [PE]
- Food Additives [CS]
- Allergens [CS]
- Dietary Proteins [CS]
NDC Crossover Matching brand name "Spearmint" or generic name "Spearmint"
| NDC | Brand Name | Generic Name |
|---|---|---|
| 36987-1742 | Spearmint | Spearmint |
| 36987-1743 | Spearmint | Spearmint |
| 36987-1744 | Spearmint | Spearmint |
| 36987-1745 | Spearmint | Spearmint |
| 54575-459 | SPEARMINT | spearmint |
Trademark Results [Spearmint]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 SPEARMINT 98752323 not registered Live/Pending |
Wm. Wrigley Jr. Company 2024-09-16 |
 SPEARMINT 98435155 not registered Live/Pending |
Wenhao Ma 2024-03-05 |
 SPEARMINT 98193313 not registered Live/Pending |
Spearmint Energy 2023-09-22 |
 SPEARMINT 98193265 not registered Live/Pending |
Spearmint Energy 2023-09-22 |
 SPEARMINT 97341761 not registered Live/Pending |
Zernicek, Clifford, J 2022-03-31 |
 SPEARMINT 88437397 not registered Live/Pending |
NOHO SOLUTIONS, INC. 2019-05-20 |
 SPEARMINT 87731809 5597414 Live/Registered |
Fran Berrick 2017-12-22 |
 SPEARMINT 86806055 not registered Dead/Abandoned |
Wm. Wrigley Jr. Company 2015-11-02 |
 SPEARMINT 86776161 not registered Dead/Abandoned |
Wm. Wrigley Jr. Company 2015-10-02 |
 SPEARMINT 86700295 not registered Dead/Abandoned |
Wm. Wrigley Jr. Company 2015-07-21 |
 SPEARMINT 86681708 not registered Dead/Abandoned |
Wm. Wrigley Jr. Company 2015-07-02 |
 SPEARMINT 77729485 3741131 Dead/Cancelled |
Ty Inc. 2009-05-05 |
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