44911-0109 : Winter Blend Oral Liquid

NDC:	44911-0109
Labeler:	Energique, Inc.
Product Type:	Human OTC Drug
Drug Name:	Winter Blend
Dosage Form:	Oral Liquid
Rev. Date:	Oct 2, 2014

NDC Package Codes:

44911-0109-1: 30 ML IN 1 BOTTLE, DROPPER (44911‑0109‑1)

Active Ingredients:

Arctostaphylos Uva-ursi Leaf
Baptisia Tinctoria Root
Bryonia Alba Root
Convallaria Majalis
Crotalus Horridus Horridus Venom
Echinacea Angustifolia
Lachesis Muta Venom
Pinus Sylvestris Leafy Twig
Potassium Chloride
Selenium
Thuja Occidentalis Leafy Twig
Viscum Album Fruiting Top

Dosage Strength:

1 [hp_X]/mL
3 [hp_X]/mL
12 [hp_X]/mL
6 [hp_X]/mL
12 [hp_X]/mL
1 [hp_X]/mL
12 [hp_X]/mL
6 [hp_X]/mL
6 [hp_X]/mL
12 [hp_X]/mL
6 [hp_X]/mL
12 [hp_X]/mL

Pharmaceutical Classes:

Increased Large Intestinal Motility [PE]
Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]
Osmotic Activity [MoA]
Osmotic Laxative [EPC]
Potassium Compounds [CS]
Potassium Salt [EPC]

NDC QR Code

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NDC 44911-0109 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.