Lipotox NDC 43857-0636

NDC codes

FDA NDC Directory

Product NDC (as listed)43857-0636Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43857-0636Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
43857-0636-1	43857063601	30 mL in 1 BOTTLE, DISPENSING (43857-0636-1)Marketed from Sep 5, 2023

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Lipotox
Generic name (nonproprietary): 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 metallicum,
Active ingredients: Squalene — 8 [hp_X]/mLCholesterol — 12 [hp_X]/mLEstradiol — 12 [hp_X]/mLProgesterone — 12 [hp_X]/mLAspartame — 30 [hp_X]/mLBenzalkonium chloride — 30 [hp_X]/mLFormaldehyde solution — 30 [hp_X]/mLMethylene chloride — 30 [hp_X]/mLMethylparaben — 30 [hp_X]/mLPropylparaben — 30 [hp_X]/mLSodium benzoate — 30 [hp_X]/mLAnhydrous trisodium citrate — 30 [hp_X]/mLTitanium dioxide — 30 [hp_X]/mLZinc oxide — 30 [hp_X]/mLArsenic trioxide — 30 [hp_X]/mLLycopodium clavatum spore — 30 [hp_X]/mLStrychnos nux-vomica seed — 30 [hp_X]/mLPhosphoric acid — 30 [hp_X]/mLPhosphorus — 30 [hp_X]/mLAcetic acid — 30 [hp_X]/mLBenzoic acid — 30 [hp_X]/mLBenzyl alcohol — 30 [hp_X]/mLBoric acid — 30 [hp_X]/mLChlorine — 30 [hp_X]/mLCortisone acetate — 30 [hp_X]/mLEugenol — 30 [hp_X]/mLEstrone — 30 [hp_X]/mLIsopropyl palmitate — 30 [hp_X]/mLLactic acid, Dl- — 30 [hp_X]/mLPetrolatum — 30 [hp_X]/mLPhenylbutazone — 30 [hp_X]/mLLead — 30 [hp_X]/mLPotassium sorbate — 30 [hp_X]/mLResorcinol — 30 [hp_X]/mLSalicylic acid — 30 [hp_X]/mLSorbitol — 30 [hp_X]/mLStearyl alcohol — 30 [hp_X]/mLXylitol — 30 [hp_X]/mLCorticotropin — 30 [hp_C]/mL
Dosage form: Liquid
Route: Oral
Labeler: BioActive Nutritional, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Sep 5, 2023
Listing expires: Dec 31, 2026
Other FDA classes: Acidifying Activity (Mechanism)Adrenocorticotropic Hormone (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Ammonium Ion Binding Activity (Mechanism)Ammonium Ion Binding Activity (Mechanism)Calcium Chelating Activity (Mechanism)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Corticosteroid Hormone Receptor Agonists (Mechanism)Decreased Coagulation Factor Activity (Physiologic effect)Decreased Copper Ion Absorption (Physiologic effect)Estradiol Congeners (Chemical structure)Estrogen Receptor Agonists (Mechanism)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Progesterone (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 43857-0636_c6b2d570-cc46-41fc-97f8-2734223ad76eSPL ID c6b2d570-cc46-41fc-97f8-2734223ad76eSPL set ID a1538692-ca00-4e52-9b7e-409767ee27e1UNII 7QWM220FJH, 97C5T2UQ7J, 4TI98Z838E, 4G7DS2Q64Y, Z0H242BBR1, F5UM2KM3W7, T0H3L6C7I5, 588X2YUY0A, A2I8C7HI9T, Z8IX2SC1OH, OJ245FE5EU, RS7A450LGA, 15FIX9V2JP, SOI2LOH54Z, S7V92P67HO, C88X29Y479, 269XH13919, E4GA8884NN, 27YLU75U4W, Q40Q9N063P, 8SKN0B0MIM, LKG8494WBH, R57ZHV85D4, 4R7X1O2820, 883WKN7W8X, 3T8H1794QW, 2DI9HA706A, 8CRQ2TH63M, 3B8D35Y7S4, 4T6H12BN9U, GN5P7K3T8S, 2P299V784P, 1VPU26JZZ4, YUL4LO94HK, O414PZ4LPZ, 506T60A25R, 2KR89I4H1Y, VCQ006KQ1E, K0U68Q2TXA
Pharmacologic class: Adrenocorticotropic Hormone; Anti-coagulant; Calculi Dissolution Agent; Copper Absorption Inhibitor; Corticosteroid; Estrogen; Nitrogen Binding Agent; Non-Standardized Plant Allergenic Extract; Pediculicide; Progesterone; Standardized Chemical Allergen

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N443857063601 followed by a unit qualifier and the quantity

Package 43857-0636-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Sep 5, 2023.

Indications (excerpt from the label)

INDICATIONS: For temporary relief of exhaustion & restlessness, metallic taste & dyspepsia & menstrual pain.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)