NDC 43772-0004 Adrenal Tincture

Chelidonium Majus, Echinacea, Glandula Suprarenalis Bovinum, Spleen, Carduus Marianus, Natrum Muriaticum

NDC Product Code 43772-0004

NDC Code: 43772-0004

Proprietary Name: Adrenal Tincture 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: Chelidonium Majus, Echinacea, Glandula Suprarenalis Bovinum, Spleen, Carduus Marianus, Natrum Muriaticum 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

  • 43772 - Synergy Formulas, Inc.
    • 43772-0004 - Adrenal Tincture

NDC 43772-0004-1

Package Description: 60 mL in 1 BOTTLE, DROPPER

NDC Product Information

Adrenal Tincture with NDC 43772-0004 is a a human over the counter drug product labeled by Synergy Formulas, Inc.. The generic name of Adrenal Tincture is chelidonium majus, echinacea, glandula suprarenalis bovinum, spleen, carduus marianus, natrum muriaticum. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Synergy Formulas, 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.

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.

Adrenal Tincture 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.

  • SODIUM CHLORIDE 12 [hp_X]/mL
  • PHOSPHORIC ACID 12 [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: Synergy Formulas, Inc.
Labeler Code: 43772
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: 04-01-2013 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: 12-31-2019 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 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.

Adrenal Tincture Product Label Images

Adrenal Tincture 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

Chelidonium Majus 3X, Echinacea 3X, Glandula Suprarenalis Bovinum 8X, 10X, 24X, Spleen (Bovine) 8X, 10X, 24X, Carduus Marianus 12X, Natrum Muriaticum 12X, Phosphoricum Acidum 12X


Provides specific sarcode support for the adrenals.  Gives temporary relief of nervous exhaustion, fatigue and forgetfulness.


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.


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

Inactive Ingredients

Demineralized Water, 25% Ethanol

Keep Out Of Reach Of Children

In case of overdose, get medical help or contact a Poison Control Center right away.

Indications And Usage

Provides specific sarcode support for the adrenals. Gives temporary relief of nervous exhaustion, fatigue and forgetfulness.


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

* Please review the disclaimer below.

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