NDC 61657-0952 Thyroid

Iodium, Badiaga, Fucus Vesiculosus, Calcareaarsenicum Iodatum, Thyroidinum, Carbonica, Pulsatilla, Baryta Carbonica,

NDC Product Code 61657-0952

NDC CODE: 61657-0952

Proprietary Name: Thyroid 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: Iodium, Badiaga, Fucus Vesiculosus, Calcareaarsenicum Iodatum, Thyroidinum, Carbonica, Pulsatilla, Baryta Carbonica, 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.

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.

  • Thyroid hormone is used to treat underactive thyroid (hypothyroidism). It is a natural product made from animal thyroid glands (usually a pig's). It replaces or provides more thyroid hormone, which is normally produced by the thyroid gland. Low thyroid hormone levels can occur naturally or when the thyroid gland is injured by radiation/medications or removed by surgery. Having enough thyroid hormone is important for maintaining normal mental and physical activity. In children, having enough thyroid hormone is important for normal mental and physical development. This medication is also used to treat other types of thyroid disorders (such as certain types of goiters, thyroid cancer) and also to test for thyroid function. This medication should not be used to treat infertility unless it is caused by low thyroid hormone levels. Older adults should discuss the risks and benefits of this medication with their doctor or pharmacist.

NDC Code Structure

  • 61657 - White Manufacturing Inc. Dba Micro-west

NDC 61657-0952-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Thyroid with NDC 61657-0952 is a a human over the counter drug product labeled by White Manufacturing Inc. Dba Micro-west. The generic name of Thyroid is iodium, badiaga, fucus vesiculosus, calcareaarsenicum iodatum, thyroidinum, carbonica, pulsatilla, baryta carbonica, . The product's dosage form is liquid and is administered via oral form.

Labeler Name: White Manufacturing Inc. Dba Micro-west

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.

Thyroid 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.

  • IODINE 12 [hp_X]/30mL
  • BARIUM CARBONATE 12 [hp_X]/30mL
  • ARSENIC TRIIODIDE 12 [hp_X]/30mL

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.

  • 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: White Manufacturing Inc. Dba Micro-west
Labeler Code: 61657
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: 08-26-1996 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: 12-31-2022 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: N - NO 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

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Thyroid Product Label Images

Thyroid 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

Active Ingredients

Arsenicum iod 12XBadiaga 12XBaryta carb 12XCalc carb 12XFucus 3XIodium 12XPulsatilla 12XThyroidinum 12X

Inactive Ingredients

Alcohol (20% v/v, Purified water



Keep Out Of Reach Of Children



INDICATIONS:For the temporary relief of mental, menses, skin, and immune system conditions associated with thyroid homeostasis


WARNING: STOP USE AND CALL A DOCTOR if symptoms persist or worsen. IF PREGNANT OR BREAST-FEEDING, consult a healthcare professional before use. CONTAINS ALCOHOL, in case of accidental overdose, consult a poison control center immediately.

Other Safety Information

OTHER INFORMATION: Tamper resistant for your protection. Use only if safety seal is intact.


DIRECTIONS: Take 6 drops orally, 4 times a day. For ages 12 to adult



* Please review the disclaimer below.