NDC 48951-3216 Carbo Chamomilla

Carbo Chamomilla

NDC Product Code 48951-3216

NDC CODE: 48951-3216

Proprietary Name: Carbo Chamomilla 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: Carbo Chamomilla 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.

Product Characteristics

BLACK (C48323)
Shape: CAPSULE (C48336)
8 MM
Score: 1

NDC Code Structure

  • 48951 - Uriel Pharmacy Inc.

NDC 48951-3216-7

Package Description: 90 CAPSULE in 1 BOTTLE, GLASS

NDC Product Information

Carbo Chamomilla with NDC 48951-3216 is a a human over the counter drug product labeled by Uriel Pharmacy Inc.. The generic name of Carbo Chamomilla is carbo chamomilla. The product's dosage form is capsule and is administered via oral form.

Dosage Form: Capsule - A solid oral dosage form consisting of a shell and a filling. The shell is composed of a single sealed enclosure, or two halves that fit together and which are sometimes sealed with a band. Capsule shells may be made from gelatin, starch, or cellulose, or other suitable materials, may be soft or hard, and are filled with solid or liquid ingredients that can be poured or squeezed.

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.

Carbo Chamomilla 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.

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.

  • ANISE OIL (UNII: 6Y89129C8H)

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: Uriel Pharmacy Inc.
Labeler Code: 48951
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: 09-01-2009 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: 12-31-2021 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 - NO 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Carbo Chamomilla Product Label Images

Carbo Chamomilla 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

Indications & Usage

Directions: FOR ORAL USE ONLY.

Dosage & Administration

Ages 12 and older: 1-2 capsules 3-4 times daily. Ages 2-11: 1 capsule 3-4 times daily. Under age 2: Consult a doctor.

Otc - Active Ingredient

Active Ingredients: Antimonite (Nat. antimony trisulfide) 3X, Chamomilla e rad. (Chamomile) 3X, Geum urbanum e rad. (Herb bennet) 3X, Absinthium ex herba (Wormwood) 5X, Gentiana e rad. (Yellow gentian) 5X, Zingiberis e rhiz. (Ginger) 5X, Arsenicum album (White arsenic) 6X, Calamus e rhiz. (Sweet flag) 6X, Piper nig. e fruct. (Black pepper) 7X

Inactive Ingredient

Inactive Ingredients: Carbo Fagi, Vegetable capsules, Anise oil, Caraway oil

Otc - Purpose

Uses: Temporarily relieves symptoms of upset stomach, diarrhea and flatulence

Otc - Keep Out Of Reach Of Children



Allergen Statement: This product was produced on equipment that also processes products that contain lactose.Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use. Do not use if safety seal is broken or missing.

Otc - Questions

Questions? Call 866.642.2858

Made with care by Uriel, East Troy, WI 53120


* Please review the disclaimer below.