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  5. NDC Package Code: 71742-0012-1 Spleen-pro T018

NDC Package 71742-0012-1 Spleen-pro T018

Spleen (suis),Arsenicum Album,Carbo Vegetabilis,Ceanothus Americanus,Chininum - 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:
71742-0012-1
Package Description:
59 mL in 1 BOTTLE, DROPPER
Product Code:
71742-0012
Proprietary Name:
Spleen-pro T018
Non-Proprietary Name:
Spleen (suis), Arsenicum Album, Carbo Vegetabilis, Ceanothus Americanus, Chininum Sulphuricum, Ignatia Amara, Iodium, Natrum Muriaticum, Nitricum Acidum, Phosphoricum Acidum, Phosphorus
Substance Name:
Activated Charcoal; Arsenic Trioxide; Ceanothus Americanus Leaf; Iodine; Nitric Acid; Phosphoric Acid; Phosphorus; Quinine Sulfate; Sodium Chloride; Strychnos Ignatii Seed; Sus Scrofa Spleen
Usage Information:
Spleen support, immune system support. Spleen support, immune system support.
11-Digit NDC Billing Format:
71742001201
Product Type:
Human Otc Drug
Labeler Name:
Guangzhou Renuma Medical Systems Co., Ltd
Dosage Form:
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • ACTIVATED CHARCOAL 12 [hp_X]/mL
  • ARSENIC TRIOXIDE 12 [hp_X]/mL
  • CEANOTHUS AMERICANUS LEAF 12 [hp_X]/mL
  • IODINE 12 [hp_X]/mL
  • NITRIC ACID 12 [hp_X]/mL
  • PHOSPHORIC ACID 12 [hp_X]/mL
  • PHOSPHORUS 12 [hp_X]/mL
  • QUININE SULFATE 12 [hp_X]/mL
  • SODIUM CHLORIDE 12 [hp_X]/mL
  • STRYCHNOS IGNATII SEED 12 [hp_X]/mL
  • SUS SCROFA SPLEEN 6 [hp_X]/mL
    • Pharmacologic Class(es):
  • Antimalarial - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    10-26-2017
    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 71742-0012-1?

    The NDC Packaged Code 71742-0012-1 is assigned to a package of 59 ml in 1 bottle, dropper of Spleen-pro T018, a human over the counter drug labeled by Guangzhou Renuma Medical Systems Co., Ltd. The product's dosage form is liquid and is administered via oral form.

    Is NDC 71742-0012 included in the NDC Directory?

    Yes, Spleen-pro T018 with product code 71742-0012 is active and included in the NDC Directory. The product was first marketed by Guangzhou Renuma Medical Systems Co., Ltd on October 26, 2017 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 71742-0012-1?

    The 11-digit format is 71742001201. 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 5-4-1 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
    5-4-171742-0012-15-4-271742-0012-01