NDC 54118-7977 Aller - Tox 11

Adrenal, Allium Cepa, Ambrosia Artemisiaefolia

NDC Product Code 54118-7977

NDC Code: 54118-7977

Proprietary Name: Aller - Tox 11 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: Adrenal, Allium Cepa, Ambrosia Artemisiaefolia 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

  • 54118 - Abco Laboratories, Inc
    • 54118-7977 - Aller - Tox 11

NDC 54118-7977-2

Package Description: 60 mL in 1 BOTTLE, DROPPER

NDC Product Information

Aller - Tox 11 with NDC 54118-7977 is a a human over the counter drug product labeled by Abco Laboratories, Inc. The generic name of Aller - Tox 11 is adrenal, allium cepa, ambrosia artemisiaefolia. The product's dosage form is solution/ drops and is administered via oral form.

Labeler Name: Abco Laboratories, Inc

Dosage Form: Solution/ Drops - A solution which is usually administered in a drop-wise fashion.

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.

Aller - Tox 11 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.

  • ONION 3 [hp_X]/60mL
  • ARSENIC TRIOXIDE 12 [hp_X]/60mL
  • COUMARIN 6 [hp_X]/60mL
  • HISTAMINE 6 [hp_X]/60mL
  • BEEF LIVER 5 [hp_X]/60mL
  • BEEF LUNG 3 [hp_X]/60mL
  • MENADIONE 5 [hp_X]/60mL
  • PHOSPHORUS 12 [hp_X]/60mL
  • PIPERINE 5 [hp_X]/60mL
  • HYALURONIDASE 9 [hp_X]/60mL
  • RUTIN 5 [hp_X]/60mL
  • SULFUR 12 [hp_X]/60mL

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: Abco Laboratories, Inc
Labeler Code: 54118
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: 11-28-2012 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: 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.

Aller - Tox 11 Product Label Images

Aller - Tox 11 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:Adrenal 3X, Allium cepa 3XAmbrosia artemisiaefolia 3XArsenicum album 12XATP 5XCoumarinum 6X, 12X Euphrasia officinalis 3XHistamine 6X, 12X, 30X, 12C, 30CLiver 5XLung 3X, 6XMenadione 5X, 12X, 30XMesenchyme 6X, 9X, 6CPhosphorus 12XPiperine 5X, 12X, 30XPollen allersode 9X, 12X, 30XPulsatilla Nigicans 12XRutin 5X, 12X, 30XSabadilla officinalis 3X, 6XSulphur 12X

Otc - Purpose

  • Homeopathic Relief of Environmental Sensitivity Symptoms

Otc - Keep Out Of Reach Of Children

  • Keep out of reach of children

Indications & Usage

  • 30 drops 2X daily or as recommended by a health care practitionerShake well before use.


  • 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.

Dosage & Administration

  • 30 drops 2X daily or as recommended by a health care practitionerShake well before use.

Inactive Ingredient

  • Reversed osmosis watervegetable glycerinalcohol (ethanol)

* Please review the disclaimer below.

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