NDC 63479-1807 R07 Pituitary

Adenosine Triphosphate Disodium, Ammonium Carbonate, Saffron, Strychnos Ignatii Seed, Magnesium Phosphate, Dibasic Trihydrate, Strychnos Nux-vomica Seed, And Veratrum Album Root

NDC Product Code 63479-1807

NDC CODE: 63479-1807

Proprietary Name: R07 Pituitary 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: Adenosine Triphosphate Disodium, Ammonium Carbonate, Saffron, Strychnos Ignatii Seed, Magnesium Phosphate, Dibasic Trihydrate, Strychnos Nux-vomica Seed, And Veratrum Album Root 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

  • 63479 - Apex Energetics Inc.

NDC 63479-1807-1

Package Description: 30 mL in 1 BOTTLE, GLASS

NDC Product Information

R07 Pituitary with NDC 63479-1807 is a a human over the counter drug product labeled by Apex Energetics Inc.. The generic name of R07 Pituitary is adenosine triphosphate disodium, ammonium carbonate, saffron, strychnos ignatii seed, magnesium phosphate, dibasic trihydrate, strychnos nux-vomica seed, and veratrum album root. The product's dosage form is solution and is administered via sublingual form.

Labeler Name: Apex Energetics Inc.

Dosage Form: Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.

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.

R07 Pituitary 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.

  • SAFFRON 1 [hp_Q]/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.

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

Administration Route(s)

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

  • Sublingual - Administration beneath the tongue.

Product Labeler Information

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

Labeler Name: Apex Energetics Inc.
Labeler Code: 63479
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: 11-15-1993 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: 12-31-2020 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.

R07 Pituitary 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


Drug Facts

Distributed by Apex Energetics, Inc.

Otc - Active Ingredient

Active IngredientsAdenosine Triphosphate (ATP)5XAmmonium Carbonicum4C 5C 6CCrocus Sativus1LMIgnatia Amara3X 6X 8X 12X 2C 3C 5C 6C 7CMagnesia Phosphorica6X 8X 12X 3C 5C 6C 7CNux Vomica3X 6X 8X 12X 3C 5C 6C 7CVeratrum Album3X 6X 8X 12X 2C 3C 5C 6C 7C

Otc - Purpose

  • For temporary relief of minor:stresssadnessmood changesforgetfulnessnervous irritability

Otc - Pregnancy Or Breast Feeding

If pregnant or breastfeeding, ask a health professional before use. Do not use if clear seal over the cap is broken or missing.

Otc - Keep Out Of Reach Of Children

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

Otc - Stop Use

Stop use and ask a doctor if stress, sadness, mood changes, forgetfulness, nervous irritability, or other symptoms do not improve within 7 days or are accompanied by fever.


Adults & children ages 12 years and over: Take 10 drops under the tongue 1-3 times a day, or as directed by your healthcare professional. Consult a physician for use in children under 12 years of age.

Inactive Ingredients

Alcohol (20% by volume), distilled water

* Please review the disclaimer below.