NDC 43857-0143

Lipotox

Squalene, Cholesterinum, Estrogen, Progesterone, Aspartame, Benzalkonium Chloride, Formalinum, Methylene Chloride

Lipotox is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Bioactive Nutritional, Inc.. The primary component is Squalene; Cholesterol; Estrone; Estriol; Estradiol; Progesterone; Aspartame; Benzalkonium Chloride; Formaldehyde; Methylene Chloride; Methylparaben; Propylparaben; Sodium Benzoate; Sodium Citrate; Titanium Dioxide; Zinc Oxide; Arsenic Acid; Lycopodium Clavatum Spore; Strychnos Nux-vomica Seed; Phosphoric Acid; Phosphorus; Corticotropin; Xylitol; Isopropyl Palmitate; Petrolatum; Salicylic Acid; Acetic Acid; Cortisone Acetate; Benzoic Acid; Lactic Acid; Eugenol; Boric Acid; Sorbitol; Potassium Sorbate; Benzyl Alcohol; Stearyl Alcohol; Resorcinol; Phenylbutazone; Lead; Chlorine.

• Product ID: 43857-0143_7256c616-0a78-4281-b531-36956c6f2651
• NDC: 43857-0143
• Product Type: Human Otc Drug
• Proprietary Name: Lipotox
• Generic Name: Squalene, Cholesterinum, Estrogen, Progesterone, Aspartame, Benzalkonium Chloride, Formalinum, Methylene Chloride
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2013-04-04
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: BioActive Nutritional, Inc.
• Substance Name: SQUALENE; CHOLESTEROL; ESTRONE; ESTRIOL; ESTRADIOL; PROGESTERONE; ASPARTAME; BENZALKONIUM CHLORIDE; FORMALDEHYDE; METHYLENE CHLORIDE; METHYLPARABEN; PROPYLPARABEN; SODIUM BENZOATE; SODIUM CITRATE; TITANIUM DIOXIDE; ZINC OXIDE; ARSENIC ACID; LYCOPODIUM CLAVATUM SPORE; STRYCHNOS NUX-VOMICA SEED; PHOSPHORIC ACID; PHOSPHORUS; CORTICOTROPIN; XYLITOL; ISOPROPYL PALMITATE; PETROLATUM; SALICYLIC ACID; ACETIC ACID; CORTISONE ACETATE; BENZOIC ACID; LACTIC ACID; EUGENOL; BORIC ACID; SORBITOL; POTASSIUM SORBATE; BENZYL ALCOHOL; STEARYL ALCOHOL; RESORCINOL; PHENYLBUTAZONE; LEAD; CHLORINE
• Active Ingredient Strength: 8 [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; [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; [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; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 43857-0143-1

30 mL in 1 BOTTLE, DROPPER (43857-0143-1)

• Marketing Start Date: 2013-04-04
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 43857-0143-1 [43857014301]

Lipotox LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2013-04-04
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
SQUALENE	8 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 1dc99bcf-e7c3-477d-9cb8-e5d2d8c8c76f
• Manufacturer:
  • BioActive Nutritional, Inc.
• UNII:
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  • OJ245FE5EU
  • 2P299V784P
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  • 27YLU75U4W

NDC Crossover Matching brand name "Lipotox" or generic name "Squalene, Cholesterinum, Estrogen, Progesterone, Aspartame, Benzalkonium Chloride, Formalinum, Methylene Chloride"

NDC	Brand Name	Generic Name
43857-0143	Lipotox	Squalene, Cholesterinum, Estrogen, Progesterone, Aspartame, Benzalkonium chloride, Formalinum, Methylene chloride
43857-0384	Lipotox	Squalene, Cholesterinum, Estradiol, Progesterone, Aspartame, Benzalkonium Chloride, Formalinum, Methylene Chloride, Methyl Paraben, Propyl Paraben, Sodium Benzoate, Sodium Citrate, Titanium Dioxide, Zincum Oxydatum, Arsenicum Album, Lycopodium Clavatum, Nux Vomica, Phosphoricum Acidum, Phosphorus, Aceticum Acidum, Adrenocorticotrophin, Benzoicum Acidum, Benzyl Alcohol, Boricum Acidum, Chlorinum, Cortisone Aceticum, Eugenol, Folliculinum, Isopropyl Palmitate, Lacticum Acidum, Petroleum Jelly