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Hay Fever
Hay Fever - 64117-176-01 - (SCHOENOCAULON OFFICINALE SEED)
Drug Information of Hay Fever
| Product NDC: | 64117-176 |
| Proprietary Name: | Hay Fever |
| Non Proprietary Name: | SCHOENOCAULON OFFICINALE SEED |
| Active Ingredient(s): | 30 [hp_C]/mL & nbsp; SCHOENOCAULON OFFICINALE SEED |
| Administration Route(s): | ORAL |
| Dosage Form(s): | PELLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Hay Fever
| Product NDC: | 64117-176 |
| Labeler Name: | Natural Health Supply |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 19980604 |
Package Information of Hay Fever
| Package NDC: | 64117-176-01 |
| Package Description: | 1.875 mL in 1 BOTTLE, GLASS (64117-176-01) |
NDC Information of Hay Fever
| NDC Code | 64117-176-01 |
| Proprietary Name | Hay Fever |
| Package Description | 1.875 mL in 1 BOTTLE, GLASS (64117-176-01) |
| Product NDC | 64117-176 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SCHOENOCAULON OFFICINALE SEED |
| Dosage Form Name | PELLET |
| Route Name | ORAL |
| Start Marketing Date | 19980604 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Natural Health Supply |
| Substance Name | SCHOENOCAULON OFFICINALE SEED |
| Strength Number | 30 |
| Strength Unit | [hp_C]/mL |
| Pharmaceutical Classes |
