1. Home
  2. Labeler Index
  3. Pro Weight Loss Inc.
  4. 70558-0007
  5. NDC Package Code: 70558-0007-1 Hunger Control

NDC Package 70558-0007-1 Hunger Control

Adenosinum Triphosphoricum Dinatrum,Adrenal Cortex (suis),Bacopa - 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:
70558-0007-1
Package Description:
30 mL in 1 BOTTLE, DROPPER
Product Code:
70558-0007
Proprietary Name:
Hunger Control
Non-Proprietary Name:
Adenosinum Triphosphoricum Dinatrum, Adrenal Cortex (suis), Bacopa Speciosa, Equol, Pantothenic Acid, Rhodiola, Stomach (suis), Chininum Sulphuricum, Iodium, Lycopodium Clavatum, Phosphorous, Dopamine Hydrochloride, Thyroidinum (suis), Cina, Serotonin (hydrochloride), Oxytocin, Gambogia, Morgan Gaertner
Substance Name:
Adenosine Triphosphate Disodium; Artemisia Cina Pre-flowering Top; Bacopa Monnieri Whole; Dopamine Hydrochloride; Equol, (+/-)-; Gamboge; Iodine; Lycopodium Clavatum Spore; Oxytocin; Pantothenic Acid; Phosphorus; Quinine Sulfate; Salmonella Enterica Subsp. Enterica Serovar Enteritidis; Sedum Roseum Root; Serotonin Hydrochloride; Sus Scrofa Adrenal Cortex; Sus Scrofa Stomach; Sus Scrofa Thyroid
Usage Information:
For temporary relief of symptoms including constant appetite, increased or insatiable hunger.****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration. For temporary relief of symptoms including constant appetite, increased or insatiable hunger.****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
11-Digit NDC Billing Format:
70558000701
Product Type:
Human Otc Drug
Labeler Name:
Pro Weight Loss Inc.
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):
  • ADENOSINE TRIPHOSPHATE DISODIUM 6 [hp_X]/mL
  • ARTEMISIA CINA PRE-FLOWERING TOP 8 [hp_X]/mL
  • BACOPA MONNIERI WHOLE 6 [hp_X]/mL
  • DOPAMINE HYDROCHLORIDE 8 [hp_X]/mL
  • EQUOL, (+/-)- 6 [hp_X]/mL
  • GAMBOGE 14 [hp_X]/mL
  • IODINE 6 [hp_X]/mL
  • LYCOPODIUM CLAVATUM SPORE 6 [hp_X]/mL
  • OXYTOCIN 12 [hp_X]/mL
  • PANTOTHENIC ACID 6 [hp_X]/mL
  • PHOSPHORUS 6 [hp_X]/mL
  • QUININE SULFATE 6 [hp_X]/mL
  • SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS 30 [hp_C]/mL
  • SEDUM ROSEUM ROOT 6 [hp_X]/mL
  • SEROTONIN HYDROCHLORIDE 8 [hp_X]/mL
  • SUS SCROFA ADRENAL CORTEX 6 [hp_X]/mL
  • SUS SCROFA STOMACH 6 [hp_X]/mL
  • SUS SCROFA THYROID 8 [hp_X]/mL
    • Pharmacologic Class(es):
  • Antimalarial - [EPC] (Established Pharmacologic Class)
  • Catecholamine - [EPC] (Established Pharmacologic Class)
  • Catecholamines - [CS]
  • Increased Uterine Smooth Muscle Contraction or Tone - [PE] (Physiologic Effect)
  • Oxytocic - [EPC] (Established Pharmacologic Class)
  • Oxytocin - [CS]
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    10-12-2020
    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 70558-0007-1?

    The NDC Packaged Code 70558-0007-1 is assigned to a package of 30 ml in 1 bottle, dropper of Hunger Control, a human over the counter drug labeled by Pro Weight Loss Inc.. The product's dosage form is liquid and is administered via oral form.

    Is NDC 70558-0007 included in the NDC Directory?

    Yes, Hunger Control with product code 70558-0007 is active and included in the NDC Directory. The product was first marketed by Pro Weight Loss Inc. on October 12, 2020 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 70558-0007-1?

    The 11-digit format is 70558000701. 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
    5-4-170558-0007-15-4-270558-0007-01