NDC 57955-6486 Fragrance And Phenolic Allergy Relief

NDC Product Code 57955-6486

NDC 57955-6486-2

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

Fragrance And Phenolic Allergy Relief with NDC 57955-6486 is a product labeled by King Bio Inc.. The generic name of Fragrance And Phenolic Allergy 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: 03-18-2016 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.

Fragrance And Phenolic Allergy Relief Product Label Images

Fragrance And Phenolic Allergy 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: Acetaldehyde, Arsenicum album, Balsamum peruvianum, Calcarea carbonica, Carbolicum acidum, Conium maculatum, Coumarinum, Corcus sativus, Histaminum hydrochloricum, Lachesis mutus, Lycopodium clavatum, Phosphorus, Sepia. Equal volumes of each ingredient in 12X, 24X, and LM1 potencies.

Indications & Usage

Uses for temporary relief of: respiratory irritations, irritation of skin, eyes and mucous membranes, headache, lethargy, nausea, mood swings.

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 years: 2 sprays 3 times per day.

Other Safety Information

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

Otc - Purpose

  • Uses for temporary relief of: respiratory irritationsirritation of skin, eyes and mucous membranesheadachelethargynauseamood swings

* Please review the disclaimer below.