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| Product NDC Code | 80897-001 | ||||||
|---|---|---|---|---|---|---|---|
| Drug Name | Athomer propolis |
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| Type | Brand | ||||||
| Pharm Class | Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC] |
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| Active Ingredients |
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| Route | NASAL | ||||||
| Dosage Form | SPRAY | ||||||
| RxCUI drug identifier | 351179 | ||||||
| Labeler Name | Nobu Baby LLC | ||||||
| Packages |
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| Check if available Online | Get Medication Prices online with Discount |
Active ingredient
A list of the active, medicinal ingredients in the drug product.Active Ingredient(s) Sodium Chloride (0.9%)
Dosage and administration
Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.Directions For the liquidation and removal of the unpleasant mucus, apply at least 4 sprayings in each nostril up to 4 times per day For preventative daily use, apply 1 to 2 sprayings in each nostril every day Suitable for repeated long-term use Shake well before each use
Inactive ingredient
A list of inactive, non-medicinal ingredients in a drug product.Inactive ingredients Purified Water, Propolis
Indications and usage
A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.Use For cleaning the nasal cavity and the removal of the unpleasant mucus. For nasal irrigation
Purpose
Information about the drug product’s indications for use.Purpose Nasal decongestant
Spl product data elements
Usually a list of ingredients in a drug product.Athomer Propolis Nasal decongestant WATER SODIUM CHLORIDE SODIUM CATION CHLORIDE ION PROPOLIS WAX
Package label principal display panel
The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.Package Label - Principal Display Panel 35 ml NDC: 80897-001-35 100 ml NDC: 80897-001-10 Inner bottle label outer package label Inner bottle label baby outer package label baby
Keep out of reach of children
Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.Keep out of reach of children.
Storage and handling
Information about safe storage and handling of the drug product.Other information or comments Store at room temperature between 68° and 77° F (20° to 25°C)
Warnings
Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.Warnings Use only as directed The use of this dispenser by more than one person may spread infection If you are pregnant or breastfeeding, seek guidance from a healthcare professional
Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API