NDC 58264-0309
A-17
Barley, Corn, Oat, White Rice, Rye, And Wheat
A-17 is a Sublingual Solution in the Human Otc Drug category. It is labeled and distributed by Dna Labs, Inc.. The primary component is Barley; Corn; Oat; White Rice; Rye; Wheat.
| Product ID | 58264-0309_9413ad69-d00a-4608-8233-cfd5047a7e7e |
| NDC | 58264-0309 |
| Product Type | Human Otc Drug |
| Proprietary Name | A-17 |
| Generic Name | Barley, Corn, Oat, White Rice, Rye, And Wheat |
| Dosage Form | Solution |
| Route of Administration | SUBLINGUAL |
| Marketing Start Date | 1990-01-01 |
| Marketing Category | UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC |
| Labeler Name | DNA Labs, Inc. |
| Substance Name | BARLEY; CORN; OAT; WHITE RICE; RYE; WHEAT |
| Active Ingredient Strength | 30 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL |
| NDC Exclude Flag | N |
| Listing Certified Through | 2019-12-31 |
Packaging
NDC 58264-0309-1
29.57 mL in 1 BOTTLE, GLASS (58264-0309-1)
| Marketing Start Date | 1990-01-01 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 58264-0309-1 [58264030901]
A-17 SOLUTION
| Marketing Category | UNAPPROVED HOMEOPATHIC |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 1990-01-01 |
| Inactivation Date | 2020-01-31 |
Drug Details
Active Ingredients
| Ingredient | Strength |
|---|---|
| BARLEY | 30 [hp_X]/mL |
OpenFDA Data
| SPL SET ID: | 41a5f109-f9b7-4c92-a965-95ecc1092ac5 |
| Manufacturer | |
| UNII |
Trademark Results [A-17]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 A-17 73164584 1104617 Dead/Expired |
PHILLIPS PETROLEUM COMPANY 1978-03-31 |
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