NDC 48951-3206 Carbo Chamomilla

Carbo Chamomilla

NDC Product Code 48951-3206

NDC Product Information

Carbo Chamomilla with NDC 48951-3206 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 powder and is administered via oral form.

Labeler Name: Uriel Pharmacy Inc

Dosage Form: Powder - An intimate mixture of dry, finely divided drugs and/or chemicals that may be intended for internal or external use.

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.

  • ACTIVATED CHARCOAL 2 [hp_X]/1
  • WORMWOOD 3 [hp_X]/1
  • MATRICARIA RECUTITA 3 [hp_X]/1
  • GENTIANA LUTEA ROOT 3 [hp_X]/1
  • AVENS EXTRACT 3 [hp_X]/1
  • BLACK PEPPER 3 [hp_X]/1
  • GINGER 3 [hp_X]/1
  • ANTIMONY TRISULFIDE 3 [hp_X]/1
  • ARSENIC TRIOXIDE 6 [hp_X]/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.

  • KAOLIN (UNII: 24H4NWX5CO)
  • ANISE OIL (UNII: 6Y89129C8H)
  • CARAWAY OIL (UNII: C2J9B08Q3I)
  • ACORUS CALAMUS ROOT (UNII: XY1K7KIQ0F)

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: 12-31-2019 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.

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

Purpose

Uses: Improves digestion; eases gas, nausea and indigestion.

Dosage & Administration

Directions: Take in a little water or sip frequently. Ages 12 and older: 1/4 teaspoon 3-4 times daily. Ages 2-11: 1/8 tsp. twice daily. Under age 2: Ask a doctor.

Otc-Active Ingredient

Active Ingredients: Carbo betulae (Birch wood charcoal) 2X, Absinthium (Wormwood) 3X, Chamomilla (Chamomile) 3X, Gentiana (Yellow gentian) 3X, Geum urb. (Herb bennet) 3X, Zingiberis (Ginger) 3X, Antimonite (Nat. antimony trisulfide) 4X, Calamus (Sweet flag) 4X, Piper nig. (Black pepper) 5X Arsenicum album (White arsenic) 6X

Inactive Ingredient

Inactive Ingredients:  Kaolin, Anise oil, Caraway oil, Calamus root.

Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN.

Do Not Use Section

Warnings: Do not use if allergic to any ingredient. Do not use if safety seal is broken or missing.

Ask Doctor Section

Consult a doctor if symptoms persist or worsen.

Pregnancy Or Breast Feeding Section

If you are pregnant or nursing, consult a doctor
before use.

Questions Section

Made with care by

Uriel Pharmacy

East Troy, WI 53120

Questions or comments?

Please call 1.866.642.2858

www.urielpharmacy.com

* Please review the disclaimer below.

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