What is NDC 17312-478?

17312-478 is the product NDC for Natural Eyes Floaters Relief, Sodium chloride 10 [hp_X]/1 + 7 more ingredients tablet, listed with the FDA by TRP Company. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Natural Eyes Floaters Relief (Chelidonium, Euphrasia, Kali sulph, Natrum muriaticum, Phosphorus, Physostigma, Sepia, Silicea).

What is the active ingredient?

Sodium chloride, Potassium sulfate, Euphrasia stricta, Physostigma venenosum seed, Silicon dioxide, Sepia officinalis juice, Chelidonium majus, Phosphorus.

TRP Company, NDC labeler code 17312. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Natural Eyes Floaters Relief?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Natural Eyes Floaters Relief NDC 17312-478

NDC codes

FDA NDC Directory

Product NDC (as listed)17312-478Labeler and product segments. Claims need a package NDC.

Product NDC at billing width17312-0478Add 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
17312-478-14	1731204781417312047814	1 BOTTLE in 1 PACKAGE (17312-478-14) / 70 TABLET in 1 BOTTLEMarketed from Apr 28, 2025

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): Natural Eyes Floaters Relief
Generic name (nonproprietary): chelidonium, euphrasia, kali sulph, natrum muriaticum, phosphorus, physostigma, sepia, silicea
Active ingredients: Sodium chloride — 10 [hp_X]/1Potassium sulfate — 10 [hp_X]/1Euphrasia stricta — 6 [hp_X]/1Physostigma venenosum seed — 12 [hp_X]/1Silicon dioxide — 12 [hp_X]/1Sepia officinalis juice — 7 [hp_X]/1Chelidonium majus — 6 [hp_X]/1Phosphorus — 12 [hp_X]/1
Dosage form: Tablet
Route: Oral
Labeler: TRP CompanyNDC labeler code 17312
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Apr 28, 2025
Listing expires: Dec 31, 2026
Other FDA classes: Increased Large Intestinal Motility (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Osmotic Activity (Mechanism)Osmotic Activity (Mechanism)Potassium Compounds (Chemical structure)
Identifiers: Product ID 17312-478_445dc839-50b1-efd8-e063-6394a90ac00bSPL ID 445dc839-50b1-efd8-e063-6394a90ac00bSPL set ID 445dc831-195e-4b25-e063-6294a90a6efdUNII 451W47IQ8X, 1K573LC5TV, C9642I91WL, CJV9E9IIOA, ETJ7Z6XBU4, QDL83WN8C2, 7E889U5RNN, 27YLU75U4W
Pharmacologic class: Osmotic Laxative; Potassium Salt

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

N417312047814 followed by a unit qualifier and the quantity

Package 17312-0478-14. 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 Nov 24, 2025.

Indications (excerpt from the label)

Uses* According to homeopathic indications these ingredients provide temporary relief from eye floaters after serious causes have been ruled out by a physician. *These statements are based upon traditional homeopathic practice. 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)

About NDC 17312-478

What is NDC 17312-478?: 17312-478 is the product NDC for Natural Eyes Floaters Relief, Sodium chloride 10 [hp_X]/1 + 7 more ingredients tablet, listed with the FDA by TRP Company. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Natural Eyes Floaters Relief (Chelidonium, Euphrasia, Kali sulph, Natrum muriaticum, Phosphorus, Physostigma, Sepia, Silicea).
What is the active ingredient?: Sodium chloride, Potassium sulfate, Euphrasia stricta, Physostigma venenosum seed, Silicon dioxide, Sepia officinalis juice, Chelidonium majus, Phosphorus.
Who is the labeler?: TRP Company, NDC labeler code 17312. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Natural Eyes Floaters Relief?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.