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Hayfever
Hayfever - 54973-9138-2 - (AMBROSIA ARTEMISIIFOLIA, EUPHRASIA STRICTA, ONION, and SCHOENOCAULON OFFICINALE SEED)
Drug Information of Hayfever
| Product NDC: | 54973-9138 |
| Proprietary Name: | Hayfever |
| Non Proprietary Name: | AMBROSIA ARTEMISIIFOLIA, EUPHRASIA STRICTA, ONION, and SCHOENOCAULON OFFICINALE SEED |
| Active Ingredient(s): | 3; 3; 3; 3 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 & nbsp; AMBROSIA ARTEMISIIFOLIA, EUPHRASIA STRICTA, ONION, and SCHOENOCAULON OFFICINALE SEED |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, SOLUBLE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Hayfever
| Product NDC: | 54973-9138 |
| Labeler Name: | Hyland's |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 19970527 |
Package Information of Hayfever
| Package NDC: | 54973-9138-2 |
| Package Description: | 100 TABLET, SOLUBLE in 1 BOTTLE, PLASTIC (54973-9138-2) |
NDC Information of Hayfever
| NDC Code | 54973-9138-2 |
| Proprietary Name | Hayfever |
| Package Description | 100 TABLET, SOLUBLE in 1 BOTTLE, PLASTIC (54973-9138-2) |
| Product NDC | 54973-9138 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | AMBROSIA ARTEMISIIFOLIA, EUPHRASIA STRICTA, ONION, and SCHOENOCAULON OFFICINALE SEED |
| Dosage Form Name | TABLET, SOLUBLE |
| Route Name | ORAL |
| Start Marketing Date | 19970527 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Hyland's |
| Substance Name | AMBROSIA ARTEMISIIFOLIA; EUPHRASIA STRICTA; ONION; SCHOENOCAULON OFFICINALE SEED |
| Strength Number | 3; 3; 3; 3 |
| Strength Unit | [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 |
| Pharmaceutical Classes |
