NDC 57955-5140 Nosebleed Relief

NDC Product Code 57955-5140

NDC 57955-5140-2

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

Nosebleed Relief with NDC 57955-5140 is a product labeled by King Bio Inc.. The generic name of Nosebleed Relief is . The product's dosage form is and is administered via form.

Labeler Name: King Bio Inc.

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)
  • ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
  • POTASSIUM SORBATE (UNII: 1VPU26JZZ4)

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: 02-01-2011 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 - INACTIVATED, the listing data was inactivated by the FDA. 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Nosebleed Relief Product Label Images

Nosebleed Relief 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 - Active Ingredient

Drug Facts​__________________________________________________________________________________________________________HPUS active ingredients: ​Ambrosia artemisiaefolia, Arnica montana, Bovista, Bryonia, Carbo vegetabilis, Ferrum phosphoricum, Hamamelis virginiana, Ipecacuanha, Mercurius vivus, Nitricum acidum, Phosphorus, Trillium pendulum​. Equal volumes of each ingredient in 10X, 30X, LM1 potencies.

Indications & Usage

Uses ​for temporary relief of nosebleeds commonly associated with irritations or strains, colds, coughing, sneezing or menses.

Inactive Ingredient

Inactive Ingredients: Bio-Energetically Enhanced™ pure water, citric acid and potassium sorbate.

Warnings

  • WarningsStop use and ask your doctor if symptoms persist or worsen.If pregnant or breast-feeding, ask a healthcare professional before use.

Otc - Keep Out Of Reach Of Children

  • Keep out of reach of children.

Dosage & Administration

  • DirectionsInitially, depress pump until primed.Spray one dose directly into mouth.Ages 12 and up: 3 sprays 3 times per day.Ages 2-12: 2 sprays 3 times per day.

Other Safety Information

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

Otc - Purpose

  • Uses for temporary relief of nosebleeds commonly associated with: irritations or strainscoldscoughingsneezing or menses

* Please review the disclaimer below.