Product NDC: | 76097-004 |
Proprietary Name: | Pollen Guard Weed Mix |
Non Proprietary Name: | Plantago lanceolata |
Active Ingredient(s): | 1 [hp_X]/5mL & nbsp; Plantago lanceolata |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 76097-004 |
Labeler Name: | Western Allergy Services Ltd. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 20111003 |
Package NDC: | 76097-004-05 |
Package Description: | 5 mL in 1 BOTTLE, UNIT-DOSE (76097-004-05) |
NDC Code | 76097-004-05 |
Proprietary Name | Pollen Guard Weed Mix |
Package Description | 5 mL in 1 BOTTLE, UNIT-DOSE (76097-004-05) |
Product NDC | 76097-004 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Plantago lanceolata |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 20111003 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Western Allergy Services Ltd. |
Substance Name | PLANTAGO LANCEOLATA POLLEN |
Strength Number | 1 |
Strength Unit | [hp_X]/5mL |
Pharmaceutical Classes |