NDC 50845-0169 Problen Estrogen And Progesterone

  1. Labeler Index
  2. Liddell Laboratories, Inc.
  3. NDC: 50845-0169 Problen Estrogen And Progesterone

NDC Product Code 50845-0169

NDC CODE: 50845-0169

Proprietary Name: Problen Estrogen And Progesterone 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: 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

  • 50845 - Liddell Laboratories, Inc.
    • 50845-0169 - Problen Estrogen And Progesterone

NDC 50845-0169-3

Package Description: 1 CARTON in 1 CARTON > 1 BOTTLE, SPRAY in 1 CARTON (50845-0169-2) > 30 mL in 1 BOTTLE, SPRAY (50845-0169-1)

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

NDC Product Information

Problen Estrogen And Progesterone with NDC 50845-0169 is a product labeled by Liddell Laboratories, Inc.. The generic name of Problen Estrogen And Progesterone is . The product's dosage form is and is administered via form.

Labeler Name: Liddell 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: Liddell Laboratories, Inc.
Labeler Code: 50845
Start Marketing Date: 01-31-2012 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: 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.

Problen Estrogen And Progesterone Product Label Images

Problen Estrogen And Progesterone 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:  Agnus castus 3X, Angelica sinensis, radix 3X, Apis mellifica 6X, Arnica montana 6X, Cimicifuga racemosa 3X, Estradiol 9C, Estriol 9C, Folliculinum 9C, Galium aparine 3X, Glycyrrhiza glabra 3X, Korean ginseng 3X, Oophorinum suis 30C, Progesterone 6X, Sepia 30C, Thuja occidentalis 6X, Viscum album 3X.

Otc - Purpose

INDICATIONS:  Temporarily supports the body to rebalance estrogen output.  Symptoms may include: mood swings, hot flashes, irritability, lack of energy.

Warnings

WARNINGS:   Not for use on children.  If symptoms continue to recur, or if sleeplessness persists continuously for more than two weeks, consult a physician.  Insomnia may be a symptom of a serious underlying medical illness.As with all medicines, if you are pregnant or breast feeding, consult a health professional before using this product.Keep out of reach of children.  In case of overdose, get medical help or contact a Poison Control Center right away.

Dosage & Administration

DIRECTIONS:  Adults: Hold the spray-top close to your open mouth and spray twice directly under your tongue, three times a day.  Some people notice improvement within two or three weeks, others take longer.

Inactive Ingredient

INACTIVE INGREDIENTS:  Organic alcohol 30% v/v, Purified water.

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.

Indications & Usage

INDICATIONS:  Temporarily supports the body to rebalance estrogen output.  Symptoms may include: mood swings, hot flashes, irritability, lack of energy.

Otc - Questions

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* Please review the disclaimer below.