NDC 43857-0636 – Lipotox

Squalene 8 [hp_X]/mL; Cholesterol 12 [hp_X]/mL; Estradiol 12 [hp_X]/mL; Progesterone 12 [hp_X]/mL; Aspartame 30 [hp_X]/mL; Benzalkonium Chloride 30 [hp_X]/mL;… · Liquid · Oral

Human Otc Drug

Product NDC43857-0636

Product details

Brand name
Lipotox
Generic name
Squalene, Cholesterinum, Estradiol, Progesterone, Aspartame, Benzalkonium Chloride, Formalinum, Methylene Chloride, Methylparaben, Propylparaben, Sodium Benzoate, Sodium Citrate, Titanium Dioxide, Zincum Oxydatum, Arsenicum Album, Lycopodium Clavatum, Nux Vomica, Phosphoricum Acidum, Phosphorus, Aceticum Acidum, Benzoicum Acidum, Benzyl Alcohol, Boricum Acidum, Chlorinum, Cortisone Aceticum, Eugenol, Folliculinum, Isopropyl Palmitate, Lacticum Acidum, Petroleum Jelly, Phenyl Butazone, Plumbum Me
Labeler
BioActive Nutritional, Inc.
Dosage form
Liquid
Route
Oral
Marketing category
UNAPPROVED HOMEOPATHIC
Marketed since
September 5, 2023
Listing expires
December 31, 2026
Pharmacologic class
Adrenocorticotropic Hormone; Anti-coagulant; Calculi Dissolution Agent; Copper Absorption Inhibitor; Corticosteroid; Estrogen; Nitrogen Binding Agent; Nitrogen Binding Agent; Non-Standardized Plant Allergenic Extract; Pediculicide; Progesterone; Standardized Chemical Allergen; Standardized Chemical Allergen; Standardized Chemical Allergen

Active ingredients

Uses, dosage, side effects and warnings for Lipotox →

Package NDC codes (1)

Package NDCDescriptionSince
43857-0636-130 mL in 1 BOTTLE, DISPENSING (43857-0636-1)Sep 5, 2023