NDC 48951-8318 Purple Coneflower

Purple Coneflower

NDC Product Information

Purple Coneflower with NDC 48951-8318 is a a human over the counter drug product labeled by Uriel Pharmacy Inc. The generic name of Purple Coneflower is purple coneflower. The product's dosage form is spray and is administered via oral form.

Labeler Name: Uriel Pharmacy Inc

Dosage Form: Spray - A liquid minutely divided as by a jet of air or steam.

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.

Purple Coneflower 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.

  • SAGE 1 [hp_X]/1
  • CALENDULA OFFICINALIS FLOWERING TOP 1 [hp_X]/1
  • ECHINACEA PALLIDA 1 [hp_X]/1
  • EUCALYPTUS GLOBULUS LEAF 1 [hp_X]/1
  • MERCURIC CYANIDE 8 [hp_X]/1
  • SILVER NITRATE 20 [hp_X]/1
  • ATROPA BELLADONNA 20 [hp_X]/1
  • SILICON DIOXIDE 20 [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.

  • ALCOHOL (UNII: 3K9958V90M)
  • WATER (UNII: 059QF0KO0R)
  • EUCALYPTUS OIL (UNII: 2R04ONI662)

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 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.

Purple Coneflower Product Label Images

Purple Coneflower 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: Temporary relieves symptoms of sore throat and mouth inflammation.

Dosage & Administration

Directions: Take up to every 1-2 hours as needed. Ages 12 and older: 2-3 sprays.  Ages 2-11: 1-2 sprays.  Under age 2: Ask a doctor.

Otc-Active Ingredient

Active Ingredients: Calendula 1X, Echinacea (Purple coneflower) 1X, Eucalyptus 1X, Salvia (Sage) 1X, Gingiva (Bovine gums) 8X, Tonsilla (Bovine tonsil) 8X, Vaucheria (Fresh water algae) 8X, Argentum nitricum (Silver nitrate) 21X, Atropa belladonna (Nightshade) 21X, Quartz (Rock crystal) 21X

Inactive Ingredient

Inactive Ingredients: Organic cane alcohol, Water, Eucalyptus oil, Gingiva, Tonsilla, Vaucheria.

Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN.

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 worsen or persist.

Pregnancy Or Breast Feeding Section

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

Questions Section

Questions? Uriel Pharmacy866 642-2858  East Troy, WI 53120 


www.urielpharmacy.com

* Please review the disclaimer below.