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  5. NDC Package Code: 68703-213-04 Shingles Remedy

NDC Package 68703-213-04 Shingles Remedy

Croton Tiglium,Natrum Muriaticum,Plantago Major,Rhus Tox,Sarsaparilla Gel Topical - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
68703-213-04
Package Description:
113 g in 1 JAR
Product Code:
68703-213
Proprietary Name:
Shingles Remedy
Non-Proprietary Name:
Croton Tiglium, Natrum Muriaticum, Plantago Major, Rhus Tox, Sarsaparilla
Substance Name:
Croton Tiglium Seed; Plantago Major; Smilax Ornata Root; Sodium Chloride; Toxicodendron Radicans Leaf
Usage Information:
Apply to affected areas as needed. Children under 12 years of age: consult a doctor before use.
11-Digit NDC Billing Format:
68703021304
Product Type:
Human Otc Drug
Labeler Name:
Silver Star Brands
Dosage Form:
Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.
Administration Route(s):
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
    • Active Ingredient(s):
  • CROTON TIGLIUM SEED 30 [hp_X]/113g
  • PLANTAGO MAJOR 30 [hp_X]/113g
  • SMILAX ORNATA ROOT 30 [hp_X]/113g
  • SODIUM CHLORIDE 30 [hp_X]/113g
  • TOXICODENDRON RADICANS LEAF 30 [hp_X]/113g
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    12-11-2017
    Listing Expiration Date:
    12-31-2025
    Exclude Flag:
    N
    Code Structure:

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 68703-213-04?

    The NDC Packaged Code 68703-213-04 is assigned to a package of 113 g in 1 jar of Shingles Remedy, a human over the counter drug labeled by Silver Star Brands. The product's dosage form is gel and is administered via topical form.

    Is NDC 68703-213 included in the NDC Directory?

    Yes, Shingles Remedy with product code 68703-213 is active and included in the NDC Directory. The product was first marketed by Silver Star Brands on December 11, 2017 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 68703-213-04?

    The 11-digit format is 68703021304. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-268703-213-045-4-268703-0213-04