NDC 43742-1321 Post-dental Visit

Chamomilla, Echinacea (angustifolia), Hamamelis Virginiana, Hypericum Perforatum, Millefolium, Calendula Officinalis, Arnica Montana, Bellis Perennis, Rhus Tox, Bryonia (alba), Clematis Vitalba, Flos, Helianthemum Nummularium, Flos, Hepar Sulphuris Calcareum, Impatiens Glandulifera, Flos, Ornithogalum Umbellatum, Flos, Prunus Cerasifera, Flos, Carbo Vegetabilis

  1. Labeler Index
  2. Deseret Biologicals, Inc.
  3. NDC: 43742-1321 Post-dental Visit

NDC Product Code 43742-1321

NDC CODE: 43742-1321

Proprietary Name: Post-dental Visit 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: Chamomilla, Echinacea (angustifolia), Hamamelis Virginiana, Hypericum Perforatum, Millefolium, Calendula Officinalis, Arnica Montana, Bellis Perennis, Rhus Tox, Bryonia (alba), Clematis Vitalba, Flos, Helianthemum Nummularium, Flos, Hepar Sulphuris Calcareum, Impatiens Glandulifera, Flos, Ornithogalum Umbellatum, Flos, Prunus Cerasifera, Flos, Carbo Vegetabilis 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.

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.
  • Drug uses not available

NDC Code Structure

  • 43742 - Deseret Biologicals, Inc.

NDC 43742-1321-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Post-dental Visit with NDC 43742-1321 is a a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Post-dental Visit is chamomilla, echinacea (angustifolia), hamamelis virginiana, hypericum perforatum, millefolium, calendula officinalis, arnica montana, bellis perennis, rhus tox, bryonia (alba), clematis vitalba, flos, helianthemum nummularium, flos, hepar sulphuris calcareum, impatiens glandulifera, flos, ornithogalum umbellatum, flos, prunus cerasifera, flos, carbo vegetabilis. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Deseret Biologicals, 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.

Post-dental Visit 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.
  • MATRICARIA RECUTITA 3 [hp_X]/mL
  • ECHINACEA ANGUSTIFOLIA 3 [hp_X]/mL
  • HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK 3 [hp_X]/mL
  • HYPERICUM PERFORATUM 3 [hp_X]/mL
  • ACHILLEA MILLEFOLIUM 3 [hp_X]/mL
  • CALENDULA OFFICINALIS FLOWERING TOP 4 [hp_X]/mL
  • ARNICA MONTANA 4 [hp_X]/mL
  • BELLIS PERENNIS 6 [hp_X]/mL
  • TOXICODENDRON PUBESCENS LEAF 6 [hp_X]/mL
  • BRYONIA ALBA ROOT 8 [hp_X]/mL
  • CLEMATIS VITALBA FLOWER 8 [hp_X]/mL
  • HELIANTHEMUM NUMMULARIUM FLOWER 8 [hp_X]/mL
  • CALCIUM SULFIDE 8 [hp_X]/mL
  • IMPATIENS GLANDULIFERA FLOWER 8 [hp_X]/mL
  • ORNITHOGALUM UMBELLATUM FLOWERING TOP 8 [hp_X]/mL
  • PRUNUS CERASIFERA FLOWER 8 [hp_X]/mL
  • ACTIVATED CHARCOAL 12 [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.
  • 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: Deseret Biologicals, Inc.
Labeler Code: 43742
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: 12-07-2018 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: 12-31-2020 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.

Post-dental Visit Product Label Images

Post-dental Visit 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:

Chamomilla 3X, Echinacea (Angustifolia) 3X, Hamamelis Virginiana 3X, Hypericum Perforatum 3X, Millefolium 3X, 6X, Calendula Officinalis 4X, Arnica Montana 4X, 12X, 30X, 200X, Bellis Perennis 6X, Rhus Tox 6X, 12X, 30X, Bryonia (Alba) 8X, Clematis Vitalba, Flos 8X, Helianthemum Nummularium, Flos 8X, Hepar Sulphuris Calcareum 8X, Impatiens Glandulifera, Flos 8X, Ornithogalum Umbellatum, Flos 8X, Prunus Cerasifera, Flos 8X, Carbo Vegetabilis 12X.

Homeopathic Indications:

For the temporary relief of symptoms related to trauma associated with a dental procedure including inflammation, swelling and pain.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

For the temporary relief of symptoms related to trauma associated with a dental procedure including inflammation, swelling and pain.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Warnings:

Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away.If pregnant or breast-feeding, ask a health professional before use.Tamper seal: "Sealed for Your Protection."Do not use if seal is broken or missing.

Keep Out Of Reach Of Children:

Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away.

Directions:

1-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.

Inactive Ingredients:

Demineralized Water, 25% Ethanol

Questions:

Dist. By: Deseret Biologicals, Inc.469 W. Parkland DriveSandy, UT www.desbio.com

Package Label Display:

DESBIONDC 43742-1321-1HOMEOPATHICPOST-DENTALVISIT1 FL OZ (30 ml)

* Please review the disclaimer below.