Cataracc NDC 55714-4847

NDC codes

FDA NDC Directory

Product NDC (as listed)55714-4847Labeler and product segments. Claims need a package NDC.

Product NDC at billing width55714-4847Add 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
55714-4847-1	55714484701	30 mL in 1 BOTTLE, GLASS (55714-4847-1)Marketed from Sep 30, 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): Cataracc
Generic name (nonproprietary): arsenicum alb., bryonia, calc. fluor., calendula, causticum, conium, euphrasia, hydrofluoricum ac., iodium, ledum, naphthalinum, nat. mur., nux vom., phos., pulsatilla, sepia, silicea, tellurium, thiosinaminum, zinc. met.
Active ingredients: Hydrofluoric acid — 15 [hp_X]/mLSodium chloride — 15 [hp_X]/mLCalendula officinalis flowering top — 15 [hp_X]/mLCausticum — 15 [hp_X]/mLCalcium fluoride — 15 [hp_X]/mLIodine — 15 [hp_X]/mLAllylthiourea — 15 [hp_X]/mLRhododendron tomentosum leafy twig — 15 [hp_X]/mLEuphrasia stricta — 15 [hp_X]/mLConium maculatum flowering top — 15 [hp_X]/mLNaphthalene — 15 [hp_X]/mLArsenic trioxide — 15 [hp_X]/mLSepia officinalis juice — 15 [hp_X]/mLBryonia alba root — 15 [hp_X]/mLAnemone pulsatilla — 15 [hp_X]/mLStrychnos nux-vomica seed — 15 [hp_X]/mLPhosphorus — 15 [hp_X]/mLZinc — 15 [hp_X]/mLSilicon dioxide — 15 [hp_X]/mLTellurium — 16 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Newton Laboratories, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Sep 30, 2022
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)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 55714-4847_eff981d9-abe5-a113-e053-2a95a90abfecSPL ID eff981d9-abe5-a113-e053-2a95a90abfecSPL set ID eff981fd-5436-7c34-e053-2a95a90a3e8eUNII RGL5YE86CZ, 451W47IQ8X, 18E7415PXQ, DD5FO1WKFU, O3B55K4YKI, 9679TC07X4, 706IDJ14B7, 877L01IZ0P, C9642I91WL, Q28R5GF371, 2166IN72UN, S7V92P67HO, QDL83WN8C2, T7J046YI2B, I76KB35JEV, 269XH13919, 27YLU75U4W, J41CSQ7QDS, ETJ7Z6XBU4, NQA0O090ZJ
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

N455714484701 followed by a unit qualifier and the quantity

Package 55714-4847-01. 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 Dec 16, 2022.

Indications (excerpt from the label)

INDICATIONS & USAGE SECTION Formulated for symptoms such as blurred vision, light sensitivity and opacities.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)