NDC 57520-0554 Chemsode

Triticum Aestivum, Glycyrrhiza Glabra, Lappa Major, Phytolacca Decandra, Rhamnus Purshiana, Trifolium Pratense, Nitricum Acidum,

NDC Product Code 57520-0554

NDC Code: 57520-0554

Proprietary Name: Chemsode What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Triticum Aestivum, Glycyrrhiza Glabra, Lappa Major, Phytolacca Decandra, Rhamnus Purshiana, Trifolium Pratense, Nitricum Acidum, What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

  • 57520 - Apotheca Company
    • 57520-0554 - Chemsode

NDC 57520-0554-1

Package Description: 60 mL in 1 BOTTLE, DROPPER

NDC Product Information

Chemsode with NDC 57520-0554 is a a human over the counter drug product labeled by Apotheca Company. The generic name of Chemsode is triticum aestivum, glycyrrhiza glabra, lappa major, phytolacca decandra, rhamnus purshiana, trifolium pratense, nitricum acidum,. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Apotheca Company

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.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Chemsode Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • WHEAT 1 [hp_X]/mL
  • RED CLOVER 3 [hp_X]/mL
  • NITRIC ACID 12 [hp_X]/mL
  • PHOSPHORIC ACID 12 [hp_X]/mL
  • BEEF LIVER 8 [hp_X]/mL
  • PORK KIDNEY 8 [hp_X]/mL
  • SUS SCROFA LYMPH 8 [hp_X]/mL
  • PHOSPHORUS 12 [hp_X]/mL
  • SALICYLIC ACID 200 [hp_X]/mL
  • CORTICOTROPIN 200 [hp_X]/mL
  • EUGENOL 200 [hp_X]/mL
  • STEARYL ALCOHOL 200 [hp_X]/mL
  • XYLITOL 200 [hp_X]/mL
  • ESTRONE 200 [hp_X]/mL
  • BENZOIC ACID 200 [hp_X]/mL
  • CHLORINE 200 [hp_X]/mL
  • SORBITOL 200 [hp_X]/mL
  • RESORCINOL 200 [hp_X]/mL
  • BENZYL ALCOHOL 200 [hp_X]/mL
  • LACTIC ACID, DL- 200 [hp_X]/mL
  • BORIC ACID 200 [hp_X]/mL
  • ACETIC ACID 200 [hp_X]/mL
  • PHENYLBUTAZONE 200 [hp_X]/mL
  • PETROLATUM 200 [hp_X]/mL
  • LEAD 200 [hp_X]/mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • WATER (UNII: 059QF0KO0R)
  • ALCOHOL (UNII: 3K9958V90M)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Apotheca Company
Labeler Code: 57520
Marketing Category: UNAPPROVED HOMEOPATHIC - What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 07-16-2010 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2018 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: E What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Chemsode Product Label Images

Chemsode Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Otc - Active Ingredient

ACTIVE INGREDIENTS:  Triticum aestivum 1X, Glycyrrhiza glabra 3X, Lappa major 3X, Phytolacca decandra 3X, Rhamnus purshiana 3X, Trifolium pratense 3X, Nitricum acidum 6X, 12X, Phosphoricum acidum 6X, 12X, Glandula suprarenalis bovinum 8X, Hepar bovinum 8X, Kidney 8X, Lymph 8X, Belladonna 12X, Lycopodium clavatum 12X, Nux vomica 12X, Phosphorus 12X, Salicylicum acidum 30X, 60X, 200X, Adrenocorticotrophin 30X, 60X, 200X, Cortisone aceticum 30X, 60X, 200X, Eugenol 30X, 60X, 200X, Stearyl alcohol 30X, 60X, 200X, Xylitol 30X, 60X, 200X, Folliculinum 30X, 60X, 200X, Benzoicum acidum 30X, 60X, 200X, Chlorinum 30X, 60X, 200X, Potassium sorbate 30X, 60X, 200X, Sorbitol 30X, 60X, 200X, Resorcinol 30X, 60X, 200X, Benzyl alcohol 30X, 60X, 200X, Lacticum acidum 30X, 60X, 200X, Isopropyl palmitate 30X, 60X, 200X, Boricum acidum 30X, 60X, 200X, Aceticum acidum 30X, 60X, 200X, Phenylbutazone 30X, 60X, 200X, Petroleum jelly 30X, 60X, 200X, Plumbum metallicum 30X, 60X, 200X.

Otc - Purpose

INDICATIONS:  Aids in homeopathic stimulation of immune response to excessive use, and homotoxic storage of drug residues; ie., antibiotics, analgesics, chemotherapies, psychotropics, antidepressants, and OTC remedies.


WARNINGS:  Keep out of reach of children.  In case of overdose, get medical help or contact a Poison Control Center right away.If pregnant or breast-feeding, ask a health professional before use.Do not use if tamper evident seal is broken or missing.

Dosage & Administration

DIRECTIONS:  10 drops orally, 3 times a day.  Consult a physician for use in children under 12 years of age.

Inactive Ingredient

INACTIVE INGREDIENTS:  Demineralized water, 25% Ethanol.

Otc - Questions

Distributed by:SYNERGY FORMULAS, INC.251 West RoadCampobello, SC 29322

* Please review the disclaimer below.

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