NDC codes

FDA NDC Directory
Product NDC (as listed)43742-2060Labeler and product segments. Claims need a package NDC.
Product NDC at billing width43742-2060Add 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 NDC11-digit (billing)PackageCopy
43742-2060-14374220600130 mL in 1 BOTTLE, DROPPER (43742-2060-1)Marketed from Sep 20, 2022

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)
boldo, chelidonium majus, sarsaparilla (smilax regelii), gelsemium sempervirens, veratrum album,beta vulgaris, ferrum metallicum, iodium, lycopodium clavatum, nux vomica, pulsatilla (pratensis), selenium metallicum, thuja occidentalis, zincum metallicum
Active ingredients
Peumus boldus leaf — 3 [hp_X]/mLChelidonium majus whole — 3 [hp_X]/mLSmilax ornata whole — 6 [hp_X]/mLGelsemium sempervirens root — 8 [hp_X]/mLVeratrum album root — 8 [hp_X]/mLBeta vulgaris whole — 12 [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
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Marketing end
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 43742-2060_fcadc2f0-a156-4408-bdb2-c7a6989f4522SPL ID fcadc2f0-a156-4408-bdb2-c7a6989f4522SPL set ID a51b65c3-1cd2-4b97-96bc-6db1dbfaf82eUNII Q4EWM09M3O, 7E889U5RNN, SJO6NF5H81, 639KR60Q1Q, QNS6W5US1Z, 4G174V5051, 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

N443742206001 followed by a unit qualifier and the quantity

Package 43742-2060-01. 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 .

Indications (excerpt from the label)

USES: • For the temporary relief of symptoms including: • bladder discomfort • perspiration • expectoration • nasal discomfort • mucus congestion • occasional constipation 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)

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