NDC 50845-0202 Pregnancy Balance

Berber Vulg, Carduus Mar, Chelidonium Maj, Podoph Pelt, Serum Anguillae, Symphoricarpus, Zingiber

NDC Product Code 50845-0202

NDC Code: 50845-0202

Proprietary Name: Pregnancy Balance 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: Berber Vulg, Carduus Mar, Chelidonium Maj, Podoph Pelt, Serum Anguillae, Symphoricarpus, Zingiber 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.
    • 50845-0202 - Pregnancy Balance

NDC 50845-0202-1

Package Description: 30 mL in 1 BOTTLE, SPRAY

NDC Product Information

Pregnancy Balance with NDC 50845-0202 is a a human over the counter drug product labeled by Liddell Laboratories, Inc.. The generic name of Pregnancy Balance is berber vulg, carduus mar, chelidonium maj, podoph pelt, serum anguillae, symphoricarpus, zingiber. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Liddell Laboratories, Inc.

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

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.

Pregnancy Balance 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.

  • BERBERIS VULGARIS ROOT BARK 6 [hp_X]/mL
  • MILK THISTLE 3 [hp_X]/mL
  • CHELIDONIUM MAJUS 6 [hp_C]/mL
  • PODOPHYLLUM 6 [hp_X]/mL
  • ANGUILLA ROSTRATA BLOOD SERUM 30 [hp_C]/mL
  • SYMPHORICARPOS ALBUS FRUIT 200 [hp_X]/mL
  • GINGER 6 [hp_X]/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.

  • 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: Liddell Laboratories, Inc.
Labeler Code: 50845
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: 03-07-2014 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: 12-31-2019 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.

Pregnancy Balance Product Label Images

Pregnancy Balance 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

Active Ingredients:

Berber vulg 6X, Carduus mar 3x, Chelidonium maj 6C, Podoph pelt 6X, Serum anguillae 30C, Symphoricarpus 200C, Zingiber 6X

Indications:

May temporarily relieve symptoms associated with pregnancy such as: morning sickness, emotional fluctuations, backaches, bladder problems and hemorrhoids.****These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

May temporarily relieve symptoms associated with pregnancy such as: morning sickness, emotional fluctuations, backaches, bladder problems and hemorrhoids.****These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

Warnings:

If symptoms persist, consult a doctor. If pregnant of breast feeding, ask a doctor before use. Keep out of reach of children. In case of overdose, get medical help or call a Posion Control Center right away. Do not use if TAMPER EVIDENT seal around neck of bottle is missing or broken.

Directions:

Adults only. Spray twice under the toung three times per day from onset of pregnancy until birth.

Inactive Ingredients:

Organic alcohol 20% v/v, Purfied water.

Keep Out Of Reach Of Children

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

Questions:

Dist. By LIDDELL LABORATORIES INC.WOODBINE, IA 51579WWW.LIDDELL.NET 1-800-460-7733

Package Label Display

ORAL SPRAYSLIDDELLLABORATORIESEST. 199455 PrgBPregnancy BalanceHOMEOPATHIC1.0 FL OZ. (30 ml) 20% organic alcohol

* Please review the disclaimer below.

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