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  5. NDC Package Code: 68770-210-42 Cataract

NDC Package 68770-210-42 Cataract

Calcium Fluoride,Tribasic Calcium Phosphate,Causticum,Jacobaea Maritima Whole,Euphrasia - 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:
68770-210-42
Package Description:
600 PELLET in 1 TUBE
Product Code:
68770-210
Proprietary Name:
Cataract
Non-Proprietary Name:
Calcium Fluoride, Tribasic Calcium Phosphate, Causticum, Jacobaea Maritima Whole, Euphrasia Stricta, Sepia Officinalis Juice, Silicon Dioxide
Substance Name:
Calcium Fluoride; Causticum; Euphrasia Stricta; Jacobaea Maritima Whole; Sepia Officinalis Juice; Silicon Dioxide; Tribasic Calcium Phosphate
Usage Information:
According to homeopathic indications, these ingredients are intended to stimulate and help the body counteract the symptoms of cataracts.
11-Digit NDC Billing Format:
68770021042
Product Type:
Human Otc Drug
Labeler Name:
Natural Ophthalmics, Inc
Dosage Form:
Pellet - A small sterile solid mass consisting of a highly purified drug (with or without excipients) made by the formation of granules, or by compression and molding.
Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • CALCIUM FLUORIDE 12 [hp_X]/1
  • CAUSTICUM 12 [hp_X]/1
  • EUPHRASIA STRICTA 7 [hp_X]/1
  • JACOBAEA MARITIMA WHOLE 6 [hp_X]/1
  • SEPIA OFFICINALIS JUICE 7 [hp_X]/1
  • SILICON DIOXIDE 13 [hp_X]/1
  • TRIBASIC CALCIUM PHOSPHATE 12 [hp_X]/1
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    04-27-2022
    Listing Expiration Date:
    12-31-2024
    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 68770-210-42?

    The NDC Packaged Code 68770-210-42 is assigned to a package of 600 pellet in 1 tube of Cataract, a human over the counter drug labeled by Natural Ophthalmics, Inc. The product's dosage form is pellet and is administered via oral form.

    Is NDC 68770-210 included in the NDC Directory?

    Yes, Cataract with product code 68770-210 is active and included in the NDC Directory. The product was first marketed by Natural Ophthalmics, Inc on April 27, 2022 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 68770-210-42?

    The 11-digit format is 68770021042. 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
    5-3-268770-210-425-4-268770-0210-42