NDC 54118-7017 Ultimate Phenolics

NDC Product Code 54118-7017

NDC 54118-7017-2

Package Description: 60 mL in 1 PACKAGE

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Ultimate Phenolics with NDC 54118-7017 is a product labeled by Abco Labratories, Inc.. The generic name of Ultimate Phenolics is . The product's dosage form is and is administered via form.

Labeler Name: Abco Labratories, Inc.

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: Abco Labratories, Inc.
Labeler Code: 54118
Start Marketing Date: 07-16-2015 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: 12-31-2017 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: I 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.

Ultimate Phenolics Product Label Images

Ultimate Phenolics 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


  • If you are pregnant, breastfeeding or taking medications consult a healthcare practitioner before use.Keep out of reach of children.Do not use if seal is missing or broken.

Otc - Keep Out Of Reach Of Children


Dosage & Administration

  • One full dropper 2x daily in water or as directed by a health care practitioner.Shake well.

Otc - Purpose

Homeopathic Support of Neurotransmitter and Sensitivities.

Indications & Usage


Inactive Ingredient

Water: Reverse osmosis, Ethyl Alcohol : Grain : 190 proof, Glycerine.

Otc - Active Ingredient

Each of the following at 6X, 12X, 30X, 200X, 12CH, 30CH, 60CH, 200CH.Acetalcholine chloride Combo, Acetaldehyde Combo, Apiolum Combo, Ascorbic Aid Combo, Apiolum Combo, Ascorbic Acid Combo, BHT Combo, Caffeic acid Combo, Candida albicans Combo, Chloragenic acid Combo, Cinnamic acid Combo, Coniferyl alcohol Combo, Coumarin Combo, Dopamin Combo, Estrogen Combo, GABA Combo, Gallic acid Combo, Histamine Combo, Indole Combo, L-Dopa Combo, Malvin Combo, Mannan Combo, Melatonin Combo, Menadione Combo, Noepinephrine Combo, Octopamine Combo, Phenylalanine Combo, Phenylisothiocyanate Combo, Phloridzin Combo, Piperin Combo, Progesterone Combo, Pyrole Combo, Quercetin Combo, Rutin Combo, Salsolinol Combo, Serotonin Combo, Taurine Combo, Testosterone Combo, Tryptophan Combo, ATP 5X, Mesenchyme 6X, 9X, 6C.

* Please review the disclaimer below.