NDC product
Natural Eyes Floaters Relief
NDC 17312-478 · TRP Company
Key facts
| Product NDC | 17312-478 |
|---|---|
| Proprietary name | Natural Eyes Floaters Relief |
| Nonproprietary name | Chelidonium, Euphrasia, Kali sulph, Natrum muriaticum, Phosphorus, Physostigma, Sepia, Silicea |
| Substances | SODIUM CHLORIDE, POTASSIUM SULFATE, EUPHRASIA STRICTA, PHYSOSTIGMA VENENOSUM SEED, SILICON DIOXIDE, SEPIA OFFICINALIS JUICE, CHELIDONIUM MAJUS, PHOSPHORUS |
| Dosage form | TABLET |
| Route | ORAL |
| Labeler | TRP Company |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC] |
| Marketing start | Apr 28, 2025 |
| Listing certified through | Dec 31, 2026 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date: