NDC 43857-0417 – Endoplex F

Black Cohosh 3 [hp_X]/mL; Fucus Vesiculosus 3 [hp_X]/mL; Glycyrrhiza Glabra 3 [hp_X]/mL; Zanthoxylum Americanum Bark 3 [hp_X]/mL; Epinephrine 8 [hp_X]/mL; Sus… · Liquid · Oral

Human Otc Drug

Product NDC43857-0417

Product details

Brand name
Endoplex F
Generic name
Cimicifuga Racemosa, Fucus Vesiculosus, Glycyrrhiza Glabra, Xanthoxylum Fraxineum, Adrenalinum, Cerebrum Suis, Hypophysis Suis, Hypothalamus (Suis), Oophorinum (Suis), Pineal (Suis), Thyroidinum (Suis), Pulsatilla (Vulgaris), Sepia
Labeler
BioActive Nutritional, Inc.
Dosage form
Liquid
Route
Oral
Marketing category
UNAPPROVED HOMEOPATHIC
Marketed since
September 29, 2016
Listing expires
December 31, 2027
Pharmacologic class
Catecholamine; Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract; alpha-Adrenergic Agonist; beta-Adrenergic Agonist

Active ingredients

Uses, dosage, side effects and warnings for Endoplex F →

Package NDC codes (1)

Package NDCDescriptionSince
43857-0417-130 mL in 1 BOTTLE, DROPPER (43857-0417-1)Sep 29, 2016