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| Product NDC Code | 69993-100 | ||||
|---|---|---|---|---|---|
| Drug Name | Maximum strength blue emu pain relief blu emu |
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| Type | Brand | ||||
| Active Ingredients |
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| Route | TOPICAL | ||||
| Dosage Form | SPRAY | ||||
| RxCUI drug identifier | 1048119 | ||||
| Application Number | part348 | ||||
| Labeler Name | NFI, 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 Trolamine salicylate 10%
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 adults and children over 12 years: • apply generously to affected area • massage into painful area until thoroughly absorbed into skin • repeat as necessary, but no more than 4 times daily children 12 years or younger: ask a doctor.
Inactive ingredient
A list of inactive, non-medicinal ingredients in a drug product.Inactive ingredients Aloe Barbadensis Leaf Juice, Caprylyl Glycol, Dimethyl Sulfone, Disodium EDTA, Emu Oil, Ethylhexylglycerin, Emu Oil, Glucosamine Sulfate, Glycerin, Glyceryl Caprylate, Lecithin, Oleic Acid, Panthenol, Phenoxyethanol, Polysorbate 20, Sorbitol, Water, Xanthan Gum.
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.Uses For the temporary relief of minor aches and pains of muscles and joints associated with: • simple backache • arthritis • strains • bruises and sprains
Purpose
Information about the drug product’s indications for use.Purpose Topical analgesic
Spl product data elements
Usually a list of ingredients in a drug product.Maximum Strength Blue Emu Pain Relief Blu Emu Trolamine Salicylate Trolamine Salicylate Salicylic Acid Aloe Caprylyl Glycol DIMETHYL SULFONE Edetate Disodium DMDM Hydantoin Emu Oil Glucosamine Sulfate Glycerin GLYCERYL MONOCAPRYLATE LECITHIN, SOYBEAN Oleic Acid Panthenol Phenoxyethanol Polysorbate 20 SORBITOL Water Xanthan Gum
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.PRINCIPAL DISPLAY PANEL - 118 ml Can Label ANY DIRECTION PAIN RELIEF SPRAY BLUE-EMU ® Continuous Spray AMERICA'S #1 EMU OIL FORMULA ODOR FREE Contains Emu Oil NET WT 4 OZ (118ml) image-01
Spl unclassified section
Information not classified as belonging to one of the other fields. Approximately 40% of labeling with effective_time between June 2009 and August 2014 have information in this field.DISTRIBUTED BY: NFI CONSUMER PRODUCTS 501 Fifth Street • Bristol, TN 37620 TOLL FREE: 1-800-432-9334 WWW.BLUE-EMU.COM
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. If swallowed, get medical help or contact a Poison Control Center right away.
Stop use
Information about when use of the drug product should be discontinued immediately and a doctor consulted. Includes information about any signs of toxicity or other reactions that would necessitate immediately discontinuing use of the product.Stop use and ask a doctor if • condition worsens • symptoms persist for more than 7 days or clear up and occur again within a few days • redness is present • irritation develops.
When using
Information about side effects that people may experience, and the substances (e.g. alcohol) or activities (e.g. operating machinery, driving a car) to avoid while using the drug product.When using this product • use only as directed • do not bandage tightly or use with a heating pad • avoid contact with eyes or mucous membranes • do not apply to wounds or damaged skin.
Pregnancy or breast feeding
Pregnancy or Breast feedingIf pregnant or breast-feeding, ask a health professional before use.
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 For external use only Allergy alert: If prone to allergic reaction from aspirin or salicylates, consult a doctor before use. When using this product • use only as directed • do not bandage tightly or use with a heating pad • avoid contact with eyes or mucous membranes • do not apply to wounds or damaged skin. Stop use and ask a doctor if • condition worsens • symptoms persist for more than 7 days or clear up and occur again within a few days • redness is present • irritation develops. If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
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