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Leader ice blue analgesic - Medication Information

Product NDC Code 70000-0260
Drug Name

Leader ice blue analgesic

Type Brand
Active Ingredients
Menthol, unspecified form 20 mg/g
Route TOPICAL
Dosage Form GEL
RxCUI drug identifier 311502
Application Number M017
Labeler Name Cardinal Health, 110 dba LEADER
Packages
Package NDC Code Description
70000-0260-1 226.8 g in 1 jar (70000-0260-1)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredients 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 ♦ Clean affected area before applying product ♦ adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily ♦ children under 2 years of age: do not use, consult a doctor

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients Ammonium Hydroxide, Blue 1, Carbomer, Copper Sulfate, Isopropyl Alcohol, Magnesium Sulfate, Sodium Hydroxide, Thymol, Water.

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 ♦ temporarily relieves minor aches and pains of muscles and joints associated with ♦ simple backache ♦ arthritis ♦ strains ♦ bruises ♦ sprains ♦ provides cooling penetrating relief

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.
Leader Ice Blue Analgesic Menthol, Unspecified Form Menthol, Unspecified Form Menthol, Unspecified Form AMMONIA DISODIUM N-ETHYL-N-4-((4-(ETHYL((3-SULFOPHENYL)METHYL)AMINO)PHENYL)(2-SULFOPHENYL)METHYLENE)-2,5-CYCLOHEXADIEN-1-YLIDENE)-3-SULFOBENZENEMETHANAMINIUM CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED CUPRIC SULFATE ANHYDROUS ISOPROPYL ALCOHOL MAGNESIUM SULFATE ANHYDROUS SODIUM HYDROXIDE THYMOL WATER

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 - 226.8 g Jar Label LEADER NDC 70000-0260-1 Ice Blue Gel Menthol 2.0% Pain Relief Gel Cooling Greaseless COMPARE TO MINERAL ICE ® active ingredient* 100% Money Back Guarantee NET WT 8 OZ (226.8 g) PRINCIPAL DISPLAY PANEL - 226.8 g Jar 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 DISTRIBUTED BY CARDINAL HEALTH DUBLIN, OHIO 43017

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 ♦ do not use with other topical pain relievers ♦ do not use with heating pads or other heating devices

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 immediately at 1-800-222-1222.

Questions

A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.
Questions or comments? 1-866-567-8600

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 consult a doctor if ♦ condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few 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.
When using this product ♦ avoid contact with the eyes ♦ do not bandage tightly ♦ do not apply to wounds or damaged skin

Pregnancy or breast feeding

Pregnancy or Breast feeding
If pregnant or breastfeeding, ask a health professional before use

Storage and handling

Information about safe storage and handling of the drug product.
Other information ♦ do not freeze ♦ store at controlled room temperature 20 degrees to 25 degrees C, in a tightly closed container ♦ store in a cool place ♦ do not use, pour, spill or store near heat or open flame

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 use ♦ do not use with other topical pain relievers ♦ do not use with heating pads or other heating devices When using this product ♦ avoid contact with the eyes ♦ do not bandage tightly ♦ do not apply to wounds or damaged skin Stop use and consult a doctor if ♦ condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days. If pregnant or breastfeeding, ask a health professional before use Keep out of reach of children . If swallowed, get medical help or contact a Poison Control Center immediately at 1-800-222-1222.

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