Glautarakt NDC 59469-131

NDC codes

FDA NDC Directory

Product NDC (as listed)59469-131Labeler and product segments. Claims need a package NDC.

Product NDC at billing width59469-0131Add 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
59469-131-10	59469013110	1 BOTTLE, GLASS in 1 BOX (59469-131-10) / 50 mL in 1 BOTTLE, GLASSMarketed from Dec 11, 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): Glautarakt
Generic name (nonproprietary): gold trichloride, solanum dulcamara top, euphrasia stricta, nitroglycerin, hedera helix flowering twig, ruta graveolens flowering top, tobacco leaf, and cynara scolymus whole
Active ingredients: Gold trichloride — 6 [hp_X]/50mLSolanum dulcamara top — 3 [hp_X]/50mLEuphrasia stricta — 2 [hp_X]/50mLNitroglycerin — 6 [hp_X]/50mLHedera helix flowering twig — 8 [hp_X]/50mLRuta graveolens flowering top — 6 [hp_X]/50mLTobacco leaf — 6 [hp_X]/50mLCynara scolymus whole — 8 [hp_X]/50mL
Dosage form: Solution/ drops
Route: Oral
Labeler: PEKANA Naturheilmittel GmbH
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Dec 11, 2008
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Nitrates (Chemical structure)Plant Proteins (Chemical structure)Vasodilation (Physiologic effect)
Identifiers: Product ID 59469-131_9ed39c86-6061-4b0b-8691-c9d6adee55f5SPL ID 9ed39c86-6061-4b0b-8691-c9d6adee55f5SPL set ID 0aac4f4f-8f71-44fa-906f-2bf35afea431UNII 15443PR153, KPS1B1162N, C9642I91WL, G59M7S0WS3, 3D10KUA6BM, N94C2U587S, 6YR2608RSU, 9N3437ZUU0
Pharmacologic class: Nitrate Vasodilator; 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

N459469013110 followed by a unit qualifier and the quantity

Package 59469-0131-10. 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 15, 2022.

Indications (excerpt from the label)

Indications For relief of occasional overexertion of the eyes. 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)