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HAY FEVER 1
HAY FEVER 1 - 64117-203-02 - (AMBROSIA ARTEMISIIFOLIA)
Drug Information of HAY FEVER 1
| Product NDC: | 64117-203 |
| Proprietary Name: | HAY FEVER 1 |
| Non Proprietary Name: | AMBROSIA ARTEMISIIFOLIA |
| Active Ingredient(s): | 30 [hp_C]/mL & nbsp; AMBROSIA ARTEMISIIFOLIA |
| Administration Route(s): | ORAL |
| Dosage Form(s): | PELLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of HAY FEVER 1
| Product NDC: | 64117-203 |
| 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 1
| Package NDC: | 64117-203-02 |
| Package Description: | 7.5 mL in 1 BOTTLE, GLASS (64117-203-02) |
NDC Information of HAY FEVER 1
| NDC Code | 64117-203-02 |
| Proprietary Name | HAY FEVER 1 |
| Package Description | 7.5 mL in 1 BOTTLE, GLASS (64117-203-02) |
| Product NDC | 64117-203 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | AMBROSIA ARTEMISIIFOLIA |
| Dosage Form Name | PELLET |
| Route Name | ORAL |
| Start Marketing Date | 19980604 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Natural Health Supply |
| Substance Name | AMBROSIA ARTEMISIIFOLIA |
| Strength Number | 30 |
| Strength Unit | [hp_C]/mL |
| Pharmaceutical Classes |
