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| Product NDC Code | 58037-204 | ||||
|---|---|---|---|---|---|
| Drug Name | Pharmacy best ice |
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| Type | Brand | ||||
| Active Ingredients |
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| Route | TOPICAL | ||||
| Dosage Form | GEL | ||||
| RxCUI drug identifier | 1039043 | ||||
| Application Number | part348 | ||||
| Labeler Name | New Pride Corp | ||||
| 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: Menthol, 1.0%
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 Adults & Children 2 years & older. Apply liberally to painful zone and massage until absorbed into the skin. Repeat 3 or 4 times daily. Do not apply to children below two years of age.
Inactive ingredient
A list of inactive, non-medicinal ingredients in a drug product.INACTIVE INGREDIENTS: Water (Aqua), Camphor, Ethyl Alcohol, Sodium Hydroxide, Carbomer, Methylchoroisothiazolinone, Methylisothiazolinone, FD&C Blue No. 1.
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 Pharmacy's Best Ice Gel to provide temporary relief of minor pains and aches in your body's joints and muscles associated with: ■ sports injuries ■ sprains ■ arthritis ■ burises
Purpose
Information about the drug product’s indications for use.Topical Analgesic
Spl product data elements
Usually a list of ingredients in a drug product.PHARMACY BEST ICE MENTHOL METHYLISOTHIAZOLINONE WATER MENTHOL MENTHOL CAMPHOR (SYNTHETIC) ISOPROPYL ALCOHOL METHYLCHLOROISOTHIAZOLINONE SODIUM HYDROXIDE CARBOMER 934 FD&C BLUE NO. 1
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.label
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. In case of accidental ingestion, seek professional advice or contact a Posion Control Center immediately.
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.if condition worsens, discontinue use of this product and consult a physician if symptoms persist for more than 7 days.
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.Do not heat in microwave, add to hot water or any container where heating water may cause splattering and result in burns. Do not use with heating devices or pads.
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. Do not apply to wound or damaged skin. Do not bandage the applied surface. Avoid contact with mucous membranes and eyes.
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