"61941-0229-4" National Drug Code (NDC)

NDC Code	61941-0229-4
Package Description	2 BLISTER PACK in 1 BOX (61941-0229-4) > 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (61941-0229-1)
Product NDC	61941-0229
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Cold-eeze
Proprietary Name Suffix	Natural Allergy Relief
Non-Proprietary 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
Usage	ORAL
Start Marketing Date	20160101
Marketing Category Name	UNAPPROVED HOMEOPATHIC
Manufacturer	ProPhase Labs, Inc.
Substance Name	ONION; EUPATORIUM PERFOLIATUM FLOWERING TOP; BUCKWHEAT; SYMPLOCARPUS FOETIDUS ROOT; SAMBUCUS NIGRA FLOWER; TUSSILAGO FARFARA LEAF; URTICA DIOICA; ZINC GLUCONATE
Strength	2; 1; 2; 2; 1; 1; 1; 2
Strength Unit	[hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1