NDC 57520-0554 Chemsode

NDC Product Code 57520-0554

This product is EXCLUDED from the official NDC directory because the listing certification is expired.

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: 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 product labeled by Apotheca Company. The generic name of Chemsode is . The product's dosage form is and is administered via form.

Labeler Name: Apotheca Company

Dosage Form: -

Product Type: 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.

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)

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
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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