NDC 68703-109 Allergyease Great Lakes

Adenosinum Cyclophosphoricum, Adrenalinum, Adrenocorticotrophin, Allium Cepa, Ambrosia Artemisiaefolia, Chelidonium Majus, Chenopodium Vulvaria, Cichorium Intybus, Cortisone Aceticum, Euphrasia Officinalis, Galphimia Glauca, Hereda Helix, Histaminum Hydrochloricum, Junglans Cinerea, Kali Muriaticum, Mucosa Nasalis Suis, Natrum Muriaticum, Pulsatilla Nuttalliana, Rna, Sabadilla, Teucrium Scorodonia

NDC Product Code 68703-109

NDC Code: 68703-109

Proprietary Name: Allergyease Great Lakes 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: Adenosinum Cyclophosphoricum, Adrenalinum, Adrenocorticotrophin, Allium Cepa, Ambrosia Artemisiaefolia, Chelidonium Majus, Chenopodium Vulvaria, Cichorium Intybus, Cortisone Aceticum, Euphrasia Officinalis, Galphimia Glauca, Hereda Helix, Histaminum Hydrochloricum, Junglans Cinerea, Kali Muriaticum, Mucosa Nasalis Suis, Natrum Muriaticum, Pulsatilla Nuttalliana, Rna, Sabadilla, Teucrium Scorodonia 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.


Code Structure
  • 68703 - Silver Star Brands, Inc
    • 68703-109 - Allergyease Great Lakes

NDC 68703-109-59

Package Description: 59 mL in 1 BOTTLE, GLASS

NDC Product Information

Allergyease Great Lakes with NDC 68703-109 is a a human over the counter drug product labeled by Silver Star Brands, Inc. The generic name of Allergyease Great Lakes is adenosinum cyclophosphoricum, adrenalinum, adrenocorticotrophin, allium cepa, ambrosia artemisiaefolia, chelidonium majus, chenopodium vulvaria, cichorium intybus, cortisone aceticum, euphrasia officinalis, galphimia glauca, hereda helix, histaminum hydrochloricum, junglans cinerea, kali muriaticum, mucosa nasalis suis, natrum muriaticum, pulsatilla nuttalliana, rna, sabadilla, teucrium scorodonia. The product's dosage form is spray and is administered via oral form.

Labeler Name: Silver Star Brands, 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.


Allergyease Great Lakes 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.

  • CHELIDONIUM MAJUS 12 [hp_X]/59mL
  • CHENOPODIUM VULVARIA 12 [hp_X]/59mL
  • CHICORY ROOT 12 [hp_X]/59mL
  • CORTISONE ACETATE 12 [hp_X]/59mL
  • EUPHRASIA STRICTA 12 [hp_X]/59mL
  • GALPHIMIA GLAUCA FLOWERING TOP 12 [hp_X]/59mL
  • HEDERA HELIX FLOWERING TWIG 12 [hp_X]/59mL
  • HISTAMINE DIHYDROCHLORIDE 12 [hp_X]/59mL
  • JUGLANS CINEREA BRANCH BARK/ROOT BARK 12 [hp_X]/59mL
  • POTASSIUM CHLORIDE 12 [hp_X]/59mL
  • SUS SCROFA NASAL MUCOSA 12 [hp_X]/59mL
  • SODIUM CHLORIDE 12 [hp_X]/59mL
  • ANEMONE PATENS 12 [hp_X]/59mL
  • SACCHAROMYCES CEREVISIAE RNA 12 [hp_X]/59mL
  • SCHOENOCAULON OFFICINALE SEED 12 [hp_X]/59mL
  • TEUCRIUM SCORODONIA FLOWERING TOP 12 [hp_X]/59mL
  • ADENOSINE CYCLIC PHOSPHATE 12 [hp_X]/59mL
  • EPINEPHRINE 12 [hp_X]/59mL
  • CORTICOTROPIN 12 [hp_X]/59mL
  • ONION 12 [hp_X]/59mL
  • AMBROSIA ARTEMISIIFOLIA 12 [hp_X]/59mL

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.

  • CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
  • POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
  • WATER (UNII: 059QF0KO0R)

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.

* Please review the disclaimer below.

Allergyease Great Lakes Product Label Images

Allergyease Great Lakes 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

Otc - Purpose

Relieves allergies common in the U.S. Great Lakes

Otc - Active Ingredient

Drug Facts


Active Ingredients:


Equal volumes of each ingredient in 12X, 30X, and LM1 potencies: Adenosinum cyclophosphoricum, Adrenalinum, Adrenocorticotrophin, Allium cepa, Ambrosia artemisiaefolia, Chelidonium majus, Chenopodium vulvaria, Cichorium intybus, Cortisone aceticum, Euphrasia officinalis, Galphimia glauca, Hereda helix, Histaminum hydrochloricum, Junglans cinerea, Kali muriaticum, Mucosa nasalis suis, Natrum muriaticum, Pulsatilla nuttalliana, RNA, Sabadilla, Teucrium scorodonia

Indications & Usage

Uses:For temporary relieves of symptoms: itchy, watery eyes, sore throat, cough, runny nose, sneezing, congestion, headaches, hoarseness, and fatigue

Warnings

Warnings:Stop use and ask a doctor if symptoms persist or worsen

Otc - Pregnancy Or Breast Feeding

If pregnant of breastfeeding, ask a health professional before use

Otc - Keep Out Of Reach Of Children

Keep this and all medication out of reach of children

Overdosage

In case of overdose, get medical help or contact a Poison Control Center right away

Dosage & Administration

Directions: Initially, depress pump until primed. Hold close to mouth and spray directly into mouth. Use 3 times daily. Use additionally as needed. Adults: 3 pump sprays. Children 2-12: 2 pump sprays

Inactive Ingredient

Inactive Ingredients: Citric acid, potassium sorbate, pure water

Information For Patients

The letters HPUS indicate that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of the Unites StatesAll Native Remedies health products are especially formulated by experts in the field of natural health and are manufactured according to the highest pharmaceutical standards for maximum safety and effectiveness. For more information, visit us at


www.nativeremedies.comDistributed byNative Remedies, LLC


6531 Park of Commerce Blvd.


Suite 160


Boca Raton, FL 33487


Phone: +1.877.289.1235


International: 1.561.999.8857


No gluten, artificial flavors, or colorants added

Storage And Handling

Tamper resistant for your protection. Use only if safety seal is intact

* Please review the disclaimer below.

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