NDC 54575-474
WATERMELON
Watermelon
WATERMELON is a Percutaneous; Subcutaneous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Allergy Laboratories, Inc.. The primary component is Watermelon.
| Product ID | 54575-474_dbe7bebd-e445-4e59-8302-e706b795fbde |
| NDC | 54575-474 |
| Product Type | Human Prescription Drug |
| Proprietary Name | WATERMELON |
| Generic Name | Watermelon |
| Dosage Form | Injection, Solution |
| Route of Administration | PERCUTANEOUS; SUBCUTANEOUS |
| Marketing Start Date | 1972-08-29 |
| Marketing Category | BLA / BLA |
| Application Number | BLA102192 |
| Labeler Name | Allergy Laboratories, Inc. |
| Substance Name | WATERMELON |
| Active Ingredient Strength | 1 g/20mL |
| Pharm Classes | Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Allergens [CS],Dietary Proteins [CS],Fruit Proteins [EXT],Cell-mediated Immunity [PE] |
| NDC Exclude Flag | E |
| Listing Certified Through | 2018-12-31 |
Packaging
NDC 54575-474-02
2 mL in 1 VIAL, MULTI-DOSE (54575-474-02)
| Marketing Start Date | 1972-08-29 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 54575-474-10 [54575047410]
WATERMELON INJECTION, SOLUTION
| Marketing Category | BLA |
| Application Number | BLA102192 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1972-08-29 |
| Inactivation Date | 2020-01-31 |
NDC 54575-474-02 [54575047402]
WATERMELON INJECTION, SOLUTION
| Marketing Category | BLA |
| Application Number | BLA102192 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1972-08-29 |
| Inactivation Date | 2020-01-31 |
NDC 54575-474-30 [54575047430]
WATERMELON INJECTION, SOLUTION
| Marketing Category | BLA |
| Application Number | BLA102192 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1972-08-29 |
| Inactivation Date | 2020-01-31 |
NDC 54575-474-50 [54575047450]
WATERMELON INJECTION, SOLUTION
| Marketing Category | BLA |
| Application Number | BLA102192 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1972-08-29 |
| Inactivation Date | 2020-01-31 |
Drug Details
Active Ingredients
| Ingredient | Strength |
|---|---|
| WATERMELON | 1 g/20mL |
OpenFDA Data
Pharmacological Class
- Non-Standardized Food Allergenic Extract [EPC]
- Increased Histamine Release [PE]
- Allergens [CS]
- Dietary Proteins [CS]
- Fruit Proteins [EXT]
- Cell-mediated Immunity [PE]
NDC Crossover Matching brand name "WATERMELON" or generic name "Watermelon"
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0268-6233 | WATERMELON | Watermelon |
| 22840-5755 | Watermelon | Citrullus lanatus |
| 36987-1378 | Watermelon | Watermelon |
| 36987-1379 | Watermelon | Watermelon |
| 36987-1380 | Watermelon | Watermelon |
| 36987-1381 | Watermelon | Watermelon |
| 49288-0598 | Watermelon | Watermelon |
| 54575-474 | WATERMELON | watermelon |
Trademark Results [WATERMELON]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 WATERMELON 97170481 not registered Live/Pending |
Xu, Yang 2021-12-14 |
 WATERMELON 90864812 not registered Live/Pending |
Table Bluff Brewing, Inc. 2021-08-04 |
 WATERMELON 87805207 5565915 Live/Registered |
Cawy Bottling Co., Inc. 2018-02-21 |
 WATERMELON 85959876 4470451 Live/Registered |
Karr, David 2013-06-14 |
WATERMELON 85959876 4470451 Live/Registered |
Dahan, Daniel 2013-06-14 |
WATERMELON 85959876 4470451 Live/Registered |
Stewart, Alexander 2013-06-14 |
WATERMELON 85959876 4470451 Live/Registered |
Griffith, Thomas 2013-06-14 |
WATERMELON 85959876 4470451 Live/Registered |
Barringer, Julianna 2013-06-14 |
 WATERMELON 85343026 4313715 Live/Registered |
Ultimate Sports 2011-06-10 |
 WATERMELON 74053360 not registered Dead/Abandoned |
Pledger, Keith Barrington 1990-04-23 |
 WATERMELON 73258874 1181455 Dead/Cancelled |
Gasterland; Hans 1980-04-21 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.