NeuropathEase NDC 68703-313

NDC codes

FDA NDC Directory

Product NDC (as listed)68703-313Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68703-0313Add 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
68703-313-02	68703031302	59 mL in 1 BOTTLE, DROPPER (68703-313-02)Marketed from Nov 19, 2018

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): NeuropathEase
Generic name (nonproprietary): agaricus musc, arsenicum alb, hypericum, phos, silicea
Active ingredients: Amanita muscaria fruiting body — 30 [hp_C]/59mLArsenic trioxide — 30 [hp_C]/59mLHypericum perforatum — 30 [hp_C]/59mLPhosphorus — 30 [hp_C]/59mLSilicon dioxide — 6 [hp_C]/59mL
Dosage form: Liquid
Route: Oral
Labeler: Silver Star Brands
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Nov 19, 2018
Listing expires: Dec 31, 2026
Identifiers: Product ID 68703-313_2ab0f647-0253-0e1c-e063-6294a90a74b2SPL ID 2ab0f647-0253-0e1c-e063-6294a90a74b2SPL set ID 7809e54a-018d-9cf6-e053-2a91aa0aedfeUNII DIF093I037, S7V92P67HO, XK4IUX8MNB, 27YLU75U4W, 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

N468703031302 followed by a unit qualifier and the quantity

Package 68703-0313-02. 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 Jan 1, 2025.

Indications (excerpt from the label)

Uses* Uses*: Homeopathic remedy temporarily relieves burning, tingling, and numbness in hands and feet. *Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)