Systemic Drainage NDC 43742-1532

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-1532Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-1532Add 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
43742-1532-1	43742153201	60 mL in 1 BOTTLE, DROPPER (43742-1532-1)Marketed from Oct 9, 2019

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): Systemic Drainage
Generic name (nonproprietary): alfalfa, avena sativa, citrus limonum, glycyrrhiza glabra, uva-ursi, taraxacum officinale, galium aparine, schisandra chinensis, solidago virgaurea, tabacum, berberis vulgaris, chelidonium majus, hepar suis, intestine (suis), kidney (suis), lung (suis), lymph node (suis), magnesium gluconate, potassium gluconate, zincum gluconicum, nux vomica, sarcolacticum acidum, lacticum acidum, tylophora asthmatica
Active ingredients: Medicago sativa whole — 1 [hp_X]/mLAvena sativa flowering top — 1 [hp_X]/mLLemon juice — 1 [hp_X]/mLGlycyrrhiza glabra — 1 [hp_X]/mLArctostaphylos uva-ursi leaf — 1 [hp_X]/mLTaraxacum officinale — 2 [hp_X]/mLGalium aparine whole — 3 [hp_X]/mLSchisandra chinensis fruit — 3 [hp_X]/mLSolidago virgaurea flowering top — 3 [hp_X]/mLTobacco leaf — 4 [hp_X]/mLBerberis vulgaris root bark — 6 [hp_X]/mLChelidonium majus whole — 6 [hp_X]/mLPork liver — 6 [hp_X]/mLPork intestine — 6 [hp_X]/mLPork kidney — 6 [hp_X]/mLSus scrofa lung — 6 [hp_X]/mLSus scrofa lymph — 6 [hp_X]/mLMagnesium gluconate — 6 [hp_X]/mLPotassium gluconate — 6 [hp_X]/mLZinc gluconate — 6 [hp_X]/mLStrychnos nux-vomica seed — 8 [hp_X]/mLLactic acid, L- — 8 [hp_X]/mLLactic acid, Dl- — 12 [hp_X]/mLTylophora indica leaf — 16 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Deseret Biologicals, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Oct 9, 2019
Marketing end: Oct 13, 2028
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Decreased Copper Ion Absorption (Physiologic effect)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Increased IgG Production (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Small Intestine Fluid/Electrolyte Absorption (Physiologic effect)Magnesium Ion Exchange Activity (Mechanism)Osmotic Activity (Mechanism)Osmotic Activity (Mechanism)Plant Proteins (Chemical structure)Plant Proteins (Chemical structure)Plant Proteins (Chemical structure)Potassium Compounds (Chemical structure)Seed Storage Proteins (Chemical structure)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
Identifiers: Product ID 43742-1532_ad6ded51-2bd0-45ae-a956-1678046a88d0SPL ID ad6ded51-2bd0-45ae-a956-1678046a88d0SPL set ID 5e54d366-4025-4131-af8c-10ac8c500af5UNII DJO934BRBD, MA9CQJ3F7F, AGN709ANTJ, 2788Z9758H, 3M5V3D1X36, 39981FM375, Z4B6561488, ABS794681C, 5405K23S50, 6YR2608RSU, 1TH8Q20J0U, 7E889U5RNN, 6EC706HI7F, 40GMI0R60L, X7BCI5P86H, 7GL3G1COB3, 33A7VYU29L, T42NAD2KHC, 12H3K5QKN9, U6WSN5SQ1Z, 269XH13919, F9S9FFU82N, 3B8D35Y7S4, WG10XM3N5R
Pharmacologic class: Calculi Dissolution Agent; Copper Absorption Inhibitor; Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract; Osmotic Laxative; Potassium Salt

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

N443742153201 followed by a unit qualifier and the quantity

Package 43742-1532-01. 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 Jan 29, 2024.

Indications (excerpt from the label)

USES: • For the temporary relief of symptoms including: • Drainage Symptoms • Low energy • Cellular Detox symptoms • Fatigue • Headache • Body Ache These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)