NDC 54118-7972 Ultimate Rescue

NDC Product Code 54118-7972

NDC 54118-7972-2

Package Description: 60 mL in 1 BOTTLE, DROPPER

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

NDC Product Information

Ultimate Rescue with NDC 54118-7972 is a product labeled by Abco Laboratories, Inc.. The generic name of Ultimate Rescue is . The product's dosage form is and is administered via form.

Labeler Name: Abco Laboratories, 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 Laboratories, Inc.
Labeler Code: 54118
Start Marketing Date: 02-28-2011 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 Rescue Product Label Images

Ultimate Rescue 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:Cherry plum 30CClematis 30CImpatiens 30CRock rose 30CStar of Bethlehem 30CATP 5XPineal 6CThymus 6C

Otc - Purpose

Support of Stress and Trauma

Otc - Keep Out Of Reach Of Children

Keep out of reach of children

Indications & Usage

Directions:30 drops 2X daily or as recommended by a health care practitioner


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.

Inactive Ingredient

Reversed osmosis watervegetable glycerinalcohol (ethanol)

Dosage & Administration

30 drops 2X daily or as recommended by a health care practitioner

* Please review the disclaimer below.