NDC 58809-111 Dayclear Allergy Immune Therapy

NDC Product Code 58809-111

NDC 58809-111-30

Package Description: 30 mL in 1 BOTTLE, DROPPER

This product is EXCLUDED from the official NDC directory because the listing certification is expired.

NDC Product Information

Dayclear Allergy Immune Therapy with NDC 58809-111 is a product labeled by Gm Pharmaceuticals, Inc. The generic name of Dayclear Allergy Immune Therapy is . The product's dosage form is and is administered via form.

Labeler Name: Gm Pharmaceuticals, Inc

Dosage Form: -

Product Type: 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.

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)

Product Labeler Information

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

Labeler Name: Gm Pharmaceuticals, Inc
Labeler Code: 58809
Start Marketing Date: 08-13-2018 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: E 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.

Dayclear Allergy Immune Therapy 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 Ingredient

Antigens 6X,12X,30X: Zones 2, 5, & 6 Grasses, Zones 2, 5, & 6 Trees, Zones 2, 5, & 6 Weeds; Herbal Drainage Remedies: Baptisia tinctoria HPUS, Echinacea 3X HPUS, Hydrastis canadensis HPUS, Myrrha HPUS, Nasturtium aquaticum HPUS, Phytolacca decandra HPUS, Trigonella foenum-graecum


Relief from sneezing, runny nose, itchy eyes and sinus congestion.


This product is a homeopathic dilution formulated to support the body's immunity for the temporary relief of allergies.


Use only as directed.

Stop Use And Ask A Doctor If

Symptoms worsen or do not improve after 5 days

If Pregnant Or Breast-Feeding,

Consult a health professional before use.

Keep Out Of Reach Of Children.

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


  • Shake well adults and children 12 and older: 10-15 drops under the tongue three times daily. children under 12 years: 6 drops under the tongue three times daily or as directed by a health care professional. Consult a physician for use in children under 12 years of age.

Inactive Ingredients:

Ethanol, purified water, stevia

* Please review the disclaimer below.