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Orca complete menthol pain reliever - Medication Information

Product NDC Code 82939-000
Drug Name

Orca complete menthol pain reliever

Type Brand
Active Ingredients
Menthol, unspecified form 20 mg/ml
Route ORAL
Dosage Form LIQUID
RxCUI drug identifier 2611702
Application Number M022
Labeler Name ORCA Products, LLC
Packages
Package NDC Code Description
82939-000-01 1 bottle, glass in 1 box (82939-000-01) / 10 ml in 1 bottle, glass
82939-000-02 1 bottle in 1 box (82939-000-02) / 13 ml in 1 bottle
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredient Menthol 2%

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 12 years of age and older: Place 8-10 drops onto ORCA Foam or similar resorbable gelatin sponge or gauze strip in a sterile fashion and apply to areas of discomfort in oral region. Guaze strip requires removal. Orca Foam soaked sponge will resorb and does not require removal. Children under 12 years of age should be supervised in use of this product. Children under 12 years of age: Consult a dentist or doctor.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients Clove oil, glycerin, guaiacol, oregano oil, peppermint oil.

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 the temporary relief of pain due to minor irritation or injury of the mouth and gums

Purpose

Information about the drug product’s indications for use.
Purpose oral pain reliever

Spl product data elements

Usually a list of ingredients in a drug product.
ORCA Complete Menthol Pain Reliever MENTHOL CLOVE OIL GLYCERIN GUAIACOL OREGANO LEAF OIL PEPPERMINT OIL MENTHOL, UNSPECIFIED FORM MENTHOL

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 Labeling: 82939-000-02 Label Print Label

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.
Drug Facts

Do not use

Information about all contraindications for use. These contraindications are absolute and are intended for situations in which consumers should not use the product unless a prior diagnosis has been established by a doctor or for situations in which certain consumers should not use the product under any circumstances regardless of whether a doctor or health professional is consulted.
Do not use this product for more than 7 days unless directed by a dentist or doctor.

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 overdose, get medical help or contact Poison Control Center right away.

Other safety information

Information about safe use and handling of the product that may not have been specified in another field.
Other information Do not use if tamperproof seal is not intact at time of first use.

Questions

A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.
Questions? 1-970-401-1138 MON-FRI 8 AM to 3 PM (CST)

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 sore mouth symptoms do not improve in 7 days irritation, pain, or redness persists or worsens swelling, rash, or fever 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 do not exceed recommended dosage.

Pregnancy or breast feeding

Pregnancy or Breast feeding
If 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 Do not use this product for more than 7 days unless directed by a dentist or doctor. When using this product do not exceed recommended dosage. Stop use and ask a doctor if sore mouth symptoms do not improve in 7 days irritation, pain, or redness persists or worsens swelling, rash, or fever develops If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact 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