61941-0229 : Cold-eeze Oral Tablet, Delayed Release


NDC: 61941-0229
Labeler: Prophase Labs, Inc.
Product Type: Human OTC Drug
Drug Name:  Cold-eeze Natural Allergy Relief
Dosage Form: Oral Tablet, Delayed Release
Rev. Date: 


Appearance:


Markings: ZA
Shapes:  Oval
Colors:  Gray
Size (mm): 2
Segments: * 1

* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines.

NDC Package Codes:

  • 61941-0229-4: 2 BLISTER PACK IN 1 BOX (61941‑0229‑4) > 10 TABLET, DELAYED RELEASE IN 1 BLISTER PACK (61941‑0229‑1)

Active Ingredients:

  • Onion
  • Eupatorium Perfoliatum Flowering Top
  • Buckwheat
  • Symplocarpus Foetidus Root
  • Sambucus Nigra Flower
  • Tussilago Farfara Leaf
  • Urtica Dioica
  • Zinc Gluconate

Dosage Strength:

  • 2 [hp_X]/1
  • 1 [hp_X]/1
  • 2 [hp_X]/1
  • 2 [hp_X]/1
  • 1 [hp_X]/1
  • 1 [hp_X]/1
  • 1 [hp_X]/1
  • 2 [hp_X]/1

Inactive Ingredients:

  • Carbomer Homopolymer Type C (Allyl Pentaerythritol Crosslinked)
  • Calcium Phosphate, Dibasic, Dihydrate
  • Magnesium Stearate
  • Methylcellulose (25 Mpa.s)
  • Cellulose, Microcrystalline
  • Silicon Dioxide
  • Stearic Acid

NDC QR Code

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.