Supren NDC 59469-060

NDC codes

FDA NDC Directory

Product NDC (as listed)59469-060Labeler and product segments. Claims need a package NDC.

Product NDC at billing width59469-0060Add 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
59469-060-10	59469006010	1 BOTTLE, GLASS in 1 BOX (59469-060-10) / 100 mL in 1 BOTTLE, GLASSMarketed from Apr 12, 2008

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): Supren
Generic name (nonproprietary): arsenic trioxide, sulfuric acid, chamaelirium luteum root, goldenseal, wood creosote, lemna minor, magnesium fluoride, and silicon dioxide
Active ingredients: Arsenic trioxide — 12 [hp_X]/100mLSulfuric acid — 8 [hp_X]/100mLChamaelirium luteum root — 12 [hp_X]/100mLGoldenseal — 12 [hp_X]/100mLWood creosote — 12 [hp_X]/100mLLemna minor whole — 12 [hp_X]/100mLMagnesium fluoride — 12 [hp_X]/100mLSilicon dioxide — 12 [hp_X]/100mL
Dosage form: Solution/ drops
Route: Oral
Labeler: PEKANA Naturheilmittel GmbH
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Apr 12, 2008
Listing expires: Dec 31, 2026
Identifiers: Product ID 59469-060_5882f99c-53c3-428c-9991-2e409eaaf9d4SPL ID 5882f99c-53c3-428c-9991-2e409eaaf9d4SPL set ID 3b34740c-b181-4f05-9858-15b7211a4c67UNII S7V92P67HO, O40UQP6WCF, DQV54Y5H3U, ZW3Z11D0JV, 3JYG22FD73, 621HHM46SV, 5N014C7IWU, ETJ7Z6XBU4

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

N459469006010 followed by a unit qualifier and the quantity

Package 59469-0060-10. 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 Dec 22, 2022.

Indications (excerpt from the label)

Indications For relief of occasional tiredness and weakness. 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)