NDC 57955-5043 Allergy And Hay Fever Reliever

NDC Product Code 57955-5043

NDC 57955-5043-2

Package Description: 59 mL in 1 BOTTLE, SPRAY

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Allergy And Hay Fever Reliever with NDC 57955-5043 is a product labeled by King Bio Inc. The generic name of Allergy And Hay Fever Reliever is . The product's dosage form is and is administered via form.

Labeler Name: King Bio 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.

  • 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: King Bio Inc
Labeler Code: 57955
Start Marketing Date: 01-05-2012 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: 12-31-2018 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: I 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 And Hay Fever Reliever Product Label Images

Allergy And Hay Fever Reliever 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

Official HPUS: Allium cepa, Ambrosia artemisiaefolia, Arsenicum album, Arum triphyllum, Arundo mauritanica, Euphrasia officinalis, Naphthalinum, Natrum muriaticum, Sabadilla and Wyethia helenioides.Reference image allergy and hay fever.jpg

Inactive Ingredient

Equal volumes of each ingredient in a Bio-Energetically Enhanced pure water base: 10X, 30X and LM1 potencies.Reference image allergy and hay fever.jpg

Purpose

  • Uses for temporary relief of allergy and hay fever symptoms:nasal and sinus congestionrunny nose sneezingcoughsore throatred, itchy or watery eyesbronchial irritationpostnasal dripReference image allergy and hay fever.jpg

Dosage And Administration

Directions: Initially, depress pump until primed. Hold close to mouth and spray directly into mouth. Use 3 times daily. Use additionally as needed.Adult Dose 3 pump spraysChildren 2 - 12 years 2 pump spraysReference image allergy and hay fever.jpg

Warnings

If symptoms persist or worsen, consult a physician. If pregnant or nursing, take only on advice of healthcare professional. Keep out of reach of children.Other: Tamper resistant for your protection. Use only if safety seal is intact.Reference image allergy and hay fever.jpg

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.Reference image allergy and hay fever.jpg

Indications And Usage

Uses for temporary relief of allergy and hay fever symptoms: nasal and sinus congestion, runny nose, sneezing, cough, sore throat, red, itchy or watery eyes, bronchial irritation, postnasal drip.Reference image allergy and hay fever.jpg

* Please review the disclaimer below.