NDC 69152-0050 Baman 40 (number 50)

Chelidonium Majus, Aethusa Cynapium

NDC Product Code 69152-0050

NDC Code: 69152-0050

Proprietary Name: Baman 40 (number 50) 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: Chelidonium Majus, Aethusa Cynapium 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

  • 69152 - Paramesh Banerji Life Sciences Llc
    • 69152-0050 - Baman 40 (number 50)

NDC 69152-0050-1

Package Description: 96 PELLET in 1 BOTTLE

NDC Product Information

Baman 40 (number 50) with NDC 69152-0050 is a a human over the counter drug product labeled by Paramesh Banerji Life Sciences Llc. The generic name of Baman 40 (number 50) is chelidonium majus, aethusa cynapium. The product's dosage form is pellet and is administered via oral form.

Labeler Name: Paramesh Banerji Life Sciences Llc

Dosage Form: Pellet - A small sterile solid mass consisting of a highly purified drug (with or without excipients) made by the formation of granules, or by compression and molding.

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.

Baman 40 (number 50) 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.

  • CHELIDONIUM MAJUS 200 [hp_C]/1
  • AETHUSA CYNAPIUM 30 [hp_C]/1

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.

  • SUCROSE (UNII: C151H8M554)
  • LACTOSE (UNII: J2B2A4N98G)

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: Paramesh Banerji Life Sciences Llc
Labeler Code: 69152
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: 11-04-2014 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: 12-31-2017 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.

Baman 40 (number 50) Product Label Images

Baman 40 (number 50) 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

Chelidonium majus 200C HPUS, Aethusa cynapium 30C HPUS

Inactive Ingredients

Sucrose, Lactose

Purpose

Relieves nausea, cough and cold

Uses

Relieves nausea, cough and cold

Warnings

If pregnant or breast feeding ask a health professional before use.

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 (1-800-222-1222) right away.

Direction

Adult or child: Take three pills daily. Leaving a gap of 30 minutes after any food or as advised by your physician.

Manufactured By

Paramesh Banerji Life Sciences, LLC220 North Center DriveNorth Brunswick, NJ 08902, USAProduct of USATel: +1-732-743-5936

* Please review the disclaimer below.

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