WINTER BLEND

Product NDC
44911-0109
11-digit product format
449110109
Labeler code
44911
Product ID
44911-0109_d4cc7185-15e0-4896-b776-24d0e3d194a9
Type
HUMAN OTC DRUG
Nonproprietary name
Echinacea (Angustifolia), Uva-Ursi, Baptisia Tinctoria, Convallaria Majalis, Kali Muriaticum, Pinus Sylvestris, Thuja Occidentalis, Bryonia, Crotalus Horridus, Lachesis Mutus, Selenium Metallicum, Viscum Album
Dosage form
LIQUID
Route
ORAL
Labeler
Energique, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2014-10-02
Substance
ARCTOSTAPHYLOS UVA-URSI LEAF; BAPTISIA TINCTORIA ROOT; BRYONIA ALBA ROOT; CONVALLARIA MAJALIS; CROTALUS HORRIDUS HORRIDUS VENOM; ECHINACEA ANGUSTIFOLIA WHOLE; LACHESIS MUTA VENOM; PINUS SYLVESTRIS LEAFY TWIG; POTASSIUM CHLORIDE; SELENIUM; THUJA OCCIDENTALIS LEAFY TWIG; VISCUM ALBUM FRUITING TOP
Active strength
1; 3; 12; 6; 12; 1; 12; 6; 6; 12; 6; 12 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmacologic 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 exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
3M5V3D1X36ARCTOSTAPHYLOS UVA-URSI LEAFARCTOSTAPHYLOS UVA-URSI LEAF
5EF0HWI5WUBAPTISIA TINCTORIA ROOTBAPTISIA TINCTORIA ROOT
T7J046YI2BBRYONIA ALBA ROOTBRYONIA ALBA ROOT
QHH4HVF5QECONVALLARIA MAJALISCONVALLARIA MAJALIS
YHA2XLJ956CROTALUS HORRIDUS HORRIDUS VENOMCROTALUS HORRIDUS HORRIDUS VENOM
VSW71SS07ILACHESIS MUTA VENOMLACHESIS MUTA VENOM
Q1RGP4UB73PINUS SYLVESTRIS LEAFY TWIGPINUS SYLVESTRIS LEAFY TWIG
660YQ98I10POTASSIUM CHLORIDE7447-40-7POTASSIUM CHLORIDE
H6241UJ22BSELENIUM7782-49-2SELENIUM
1NT28V9397THUJA OCCIDENTALIS LEAFY TWIGTHUJA OCCIDENTALIS LEAFY TWIG
BK9092J5MPVISCUM ALBUM FRUITING TOPVISCUM ALBUM FRUITING TOP

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
44911-0109-14491101090130 mL in 1 BOTTLE, DROPPER (44911-0109-1) 30 ml2014-10-02NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
DRUG FACTS:Energique, Inc. | Apotheca Company2024-07-12HUMAN OTC DRUG LABEL6