Systemic Detox NDC 43742-1660

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-1660Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-1660Add 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
43742-1660-1	43742166001	30 mL in 1 BOTTLE, DROPPER (43742-1660-1)Marketed from Oct 5, 2020

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 Detox
Generic name (nonproprietary): beta vulgaris, boldo, chelidonium majus, sarsaparilla (smilax regelii), gelsemium sempervirens, veratrum album, ferrum metallicum, iodium, lycopodium clavatum, nux vomica, pulsatilla (pratensis), selenium metallicum, thuja occidentalis, zincum metallicum
Active ingredients: Beta vulgaris — 3 [hp_X]/mLPeumus boldus leaf — 3 [hp_X]/mLChelidonium majus — 3 [hp_X]/mLSmilax ornata whole — 6 [hp_X]/mLGelsemium sempervirens root — 8 [hp_X]/mLVeratrum album root — 8 [hp_X]/mLIron — 12 [hp_X]/mLIodine — 12 [hp_X]/mLLycopodium clavatum spore — 12 [hp_X]/mLStrychnos nux-vomica seed — 12 [hp_X]/mLPulsatilla pratensis whole — 12 [hp_X]/mLSelenium — 12 [hp_X]/mLThuja occidentalis leafy twig — 12 [hp_X]/mLZinc — 12 [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 5, 2020
Marketing end: Oct 12, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 43742-1660_ec70c9b8-a5a8-4130-911d-fad31622c447SPL ID ec70c9b8-a5a8-4130-911d-fad31622c447SPL set ID 4a76f34f-359b-448c-8b95-5997e7645f72UNII 4G174V5051, Q4EWM09M3O, 7E889U5RNN, SJO6NF5H81, 639KR60Q1Q, QNS6W5US1Z, E1UOL152H7, 9679TC07X4, C88X29Y479, 269XH13919, 8E272251DI, H6241UJ22B, 1NT28V9397, J41CSQ7QDS
Pharmacologic class: Non-Standardized Plant Allergenic Extract

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

N443742166001 followed by a unit qualifier and the quantity

Package 43742-1660-01. 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 Jun 21, 2022.

Indications (excerpt from the label)

HOMEOPATHIC INDICATIONS: For temporary relief of symptoms related to excretory dysfunction including mucous congestion.** **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)