NDC 71753-2012 Allergy Escape

Allium Cepa, Apis Mellifica, Euphrasia Officinalis, Kali Iodatum, Naphthalinum, Sabadilla, Wyethia Helenoides, Histaminum Hydrochloricum

NDC Product Code 71753-2012

NDC Code: 71753-2012

Proprietary Name: Allergy Escape 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: Allium Cepa, Apis Mellifica, Euphrasia Officinalis, Kali Iodatum, Naphthalinum, Sabadilla, Wyethia Helenoides, Histaminum Hydrochloricum 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

  • 71753 - Ratis, Llc
    • 71753-2012 - Allergy Escape

NDC 71753-2012-1

Package Description: 30 mL in 1 BOTTLE, SPRAY

NDC Product Information

Allergy Escape with NDC 71753-2012 is a a human over the counter drug product labeled by Ratis, Llc. The generic name of Allergy Escape is allium cepa, apis mellifica, euphrasia officinalis, kali iodatum, naphthalinum, sabadilla, wyethia helenoides, histaminum hydrochloricum. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Ratis, Llc

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.

Allergy Escape 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.

  • ONION 8 [hp_X]/mL
  • APIS MELLIFERA 8 [hp_X]/mL
  • EUPHRASIA STRICTA 8 [hp_X]/mL
  • POTASSIUM IODIDE 8 [hp_X]/mL
  • NAPHTHALENE 8 [hp_X]/mL
  • SCHOENOCAULON OFFICINALE SEED 8 [hp_X]/mL
  • WYETHIA HELENIOIDES ROOT 8 [hp_X]/mL
  • HISTAMINE DIHYDROCHLORIDE 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)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • 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.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Ratis, Llc
Labeler Code: 71753
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: 04-10-2019 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.

Allergy Escape Product Label Images

Allergy Escape 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:

Allium Cepa 8X, Apis Mellifica 8X, Euphrasia Officinalis 8X, Kali Iodatum 8X, Naphthalinum 8X, Sabadilla 8X, Wyethia Helenoides 8X, Histaminum Hydrochloricum 8X.

Uses:

Temporarily relieves seasonal and environmental allergies such as runny nose, itchy eyes, sinus pressure, and puffy skin.****These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

Warnings:

For oral use only.If pregnant or breast-feeding, or if symptoms persist or worsen or worsen, ask a health care professional.Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.Do not use if tamper evident seal is broken or missing.

Keep Out Of Reach Of Children:

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

Directions:

Adults: 2 sprays 3 times a day or as needed. Children 2-12: 1 spray as needed. For children 12 and under, consult a doctor.

Indications:

Temporarily relieves seasonal and environmental allergies such as runny nose, itchy eyes, sinus pressure, and puffy skin.****These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

Inactive Ingredients:

Demineralized Water, Glycerin 50%, Organic Ethanol 10%

Questions:

Comments? VisitHomeopathyStore.comor call (888) 405-7551.Distributed by:Ratis, LLC, 211 E.Lombard St, STE 303,Baltimore, MD 21202

Package Label Display:

NDC 71753-2012-1Anna'sREMEDIESAllergy EscapeALLERGY RELIEF**HOMEOPATHIC ORAL SPRAY1 FL. OZ (30ML)

* Please review the disclaimer below.

Previous Code
71753-2010
Next Code
71753-9001