NDC codes

FDA NDC Directory
Product NDC (as listed)59469-305Labeler and product segments. Claims need a package NDC.
Product NDC at billing width59469-0305Add 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
59469-305-10594690305101 BOTTLE, GLASS in 1 BOX (59469-305-10) / 50 mL in 1 BOTTLE, GLASSMarketed from Jun 24, 2019
59469-305-40594690305401 BOTTLE, GLASS in 1 BOX (59469-305-40) / 100 mL in 1 BOTTLE, GLASSMarketed from Jun 24, 2019

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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)
Dalektro N
Generic name (nonproprietary)
silver nitrate, oyster shell calcium carbonate, crude, cobaltous nitrate hexahydrate, cupric acetate, iron, potassium carbonate, magnesium chloride, manganese acetate tetrahydrate, selenium, silicon dioxide, and zinc phosphide
Active ingredients
Silver nitrate — 6 [hp_X]/100mLOyster shell calcium carbonate, Crude — 6 [hp_X]/100mLCobaltous nitrate hexahydrate — 6 [hp_X]/100mLCupric acetate — 12 [hp_X]/100mLIron — 6 [hp_X]/100mLPotassium carbonate — 4 [hp_X]/100mLMagnesium chloride — 4 [hp_X]/100mLManganese acetate tetrahydrate — 8 [hp_X]/100mLSelenium — 12 [hp_X]/100mLSilicon dioxide — 12 [hp_X]/100mLZinc phosphide — 12 [hp_X]/100mL
Dosage form
Solution/ drops
Route
Oral
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
Other FDA classes
Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Small Intestine Fluid/Electrolyte Absorption (Physiologic effect)Magnesium Ion Exchange Activity (Mechanism)Magnetic Resonance Contrast Activity (Mechanism)Osmotic Activity (Mechanism)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
Identifiers
Product ID 59469-305_7ee0a73a-1bb7-4e4e-80b2-d1ef6920c069SPL ID 7ee0a73a-1bb7-4e4e-80b2-d1ef6920c069SPL set ID 2b39ce30-54ff-4586-bda1-d9410140b26eUNII 95IT3W8JZE, 2E32821G6I, 2H2166872F, 39M11XPH03, E1UOL152H7, BQN1B9B9HA, 02F3473H9O, 9TO51D176N, H6241UJ22B, ETJ7Z6XBU4, 813396S1PC
Pharmacologic class
Calculi Dissolution Agent; Osmotic Laxative; Paramagnetic Contrast Agent

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

N459469030510 followed by a unit qualifier and the quantity

Package 59469-0305-10. 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)

Indications Homeopathically processed minerals to help reduce minor stress. Application of this homeopathic remedy for the designated usage is exclusively based on homeopathic experience. With severe forms of this disease, a clinically proven therapy is indicated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

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