NDC 61941-0229
Cold-EEZE Natural Allergy Relief
Onion, Eupatorium Perfoliatum Flowering Top, Buckwheat, Symplocarpus Foetidus Root, Sambucus Nigra Flower, Tussilago Farfara Leaf, Urtica Dioica, And Zinc Gluconate
Cold-EEZE Natural Allergy Relief is a Oral Tablet, Delayed Release in the Human Otc Drug category. It is labeled and distributed by Prophase Labs, Inc.. The primary component is Onion; Eupatorium Perfoliatum Flowering Top; Buckwheat; Symplocarpus Foetidus Root; Sambucus Nigra Flower; Tussilago Farfara Leaf; Urtica Dioica; Zinc Gluconate.
| Product ID | 61941-0229_7f819f4d-23b8-4b25-b6ae-f8755914db72 |
| NDC | 61941-0229 |
| Product Type | Human Otc Drug |
| Proprietary Name | Cold-EEZE Natural Allergy Relief |
| Generic Name | Onion, Eupatorium Perfoliatum Flowering Top, Buckwheat, Symplocarpus Foetidus Root, Sambucus Nigra Flower, Tussilago Farfara Leaf, Urtica Dioica, And Zinc Gluconate |
| Dosage Form | Tablet, Delayed Release |
| Route of Administration | ORAL |
| Marketing Start Date | 2016-01-01 |
| Marketing Category | UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC |
| Labeler Name | ProPhase Labs, Inc. |
| Substance Name | ONION; EUPATORIUM PERFOLIATUM FLOWERING TOP; BUCKWHEAT; SYMPLOCARPUS FOETIDUS ROOT; SAMBUCUS NIGRA FLOWER; TUSSILAGO FARFARA LEAF; URTICA DIOICA; ZINC GLUCONATE |
| Active Ingredient Strength | 2 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 |
| NDC Exclude Flag | E |
| Listing Certified Through | 2017-12-31 |
Packaging
NDC 61941-0229-4
2 BLISTER PACK in 1 BOX (61941-0229-4) > 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (61941-0229-1)
| Marketing Start Date | 2016-01-01 |
| NDC Exclude Flag | N |
| Sample Package? | N |
NDC SPL Data Element Entries
NDC 61941-0229-4 [61941022904]
Cold-EEZE Natural Allergy Relief TABLET, DELAYED RELEASE
| Marketing Category | UNAPPROVED HOMEOPATHIC |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2016-01-01 |
| Inactivation Date | 2020-01-31 |
NDC 61941-0229-1 [61941022901]
Cold-EEZE Natural Allergy Relief TABLET, DELAYED RELEASE
| Marketing Category | UNAPPROVED HOMEOPATHIC |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2016-01-01 |
Drug Details
Active Ingredients
| Ingredient | Strength |
|---|---|
| ONION | 2 [hp_X]/1 |
OpenFDA Data
| SPL SET ID: | aa3db5f9-cade-4d4f-b928-a619a6813391 |
| Manufacturer | |
| UNII |
Trademark Results [Cold-EEZE]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 COLD-EEZE 88294220 5839399 Live/Registered |
Mylan Consumer Healthcare, Inc. 2019-02-08 |
 COLD-EEZE 74405322 1838542 Live/Registered |
MYLAN CONSUMER HEALTHCARE INC. 1993-06-24 |
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