| Product NDC: | 76097-003 |
| Proprietary Name: | Pollen Guard Ragweed |
| Non Proprietary Name: | Ambrosia Artemisiaefolia |
| Active Ingredient(s): | 1 [hp_X]/5mL & nbsp; Ambrosia Artemisiaefolia |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 76097-003 |
| Labeler Name: | Western Allergy Services Ltd. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20111003 |
| Package NDC: | 76097-003-05 |
| Package Description: | 5 mL in 1 BOTTLE, UNIT-DOSE (76097-003-05) |
| NDC Code | 76097-003-05 |
| Proprietary Name | Pollen Guard Ragweed |
| Package Description | 5 mL in 1 BOTTLE, UNIT-DOSE (76097-003-05) |
| Product NDC | 76097-003 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Ambrosia Artemisiaefolia |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20111003 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Western Allergy Services Ltd. |
| Substance Name | AMBROSIA ARTEMISIIFOLIA |
| Strength Number | 1 |
| Strength Unit | [hp_X]/5mL |
| Pharmaceutical Classes |