Shingles Remedy NDC 68703-213

NDC codes

FDA NDC Directory

Product NDC (as listed)68703-213Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68703-0213Add 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
68703-213-04	68703021304	113 g in 1 JAR (68703-213-04)Marketed from Dec 11, 2017

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): Shingles Remedy
Generic name (nonproprietary): croton tiglium, natrum muriaticum, plantago major, rhus tox, sarsaparilla
Active ingredients: Plantago major — 30 [hp_X]/113gSodium chloride — 30 [hp_X]/113gCroton tiglium seed — 30 [hp_X]/113gToxicodendron radicans leaf — 30 [hp_X]/113gSmilax ornata root — 30 [hp_X]/113g
Dosage form: Gel
Route: Topical
Labeler: Silver Star Brands
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Dec 11, 2017
Listing expires: Dec 31, 2026
Identifiers: Product ID 68703-213_2ab0cefe-a1bc-de08-e063-6294a90a3146SPL ID 2ab0cefe-a1bc-de08-e063-6294a90a3146SPL set ID 5d65c997-f5dc-4dee-e053-2a91aa0ac319UNII W2469WNO6U, 451W47IQ8X, 0HK2GZK66E, CDH3461U7L, 2H1576D5WG

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. Topical products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N468703021304 followed by a unit qualifier and the quantity

Package 68703-0213-04. 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 Indications*: May temporarily relieve signs and symptoms associated with shingles, including stinging pain, skin lesions, itching and burning associated with herpetic eruptions and infections. *As per various homeopathic materia medicas. These indications have not been evaluated by the FDA, and product has not been clinically tested.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)