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Target up and up pain relief menthol topical analgesic roll-on - Medication Information

Product NDC Code 11673-261
Drug Name

Target up and up pain relief menthol topical analgesic roll-on

Type Brand
Active Ingredients
Menthol, unspecified form 40 mg/ml
Route TOPICAL
Dosage Form GEL
RxCUI drug identifier 415974
Application Number M017
Labeler Name TARGET CORPORATION
Packages
Package NDC Code Description
11673-261-03 89 ml in 1 bottle, with applicator (11673-261-03)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredient Menthol 4%

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 2 years of age and older: Apply to affected area not more than 3 to 4 times daily. Massage not necessary. Wash hands after use with cool water. 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 Aloe Barbadensis Leaf Extract, Aminomethyl Propanol, Arctium Lappa Root (Burdock) Extract, Arnica Montana Flower Extract, Blue 1, Boswellia Carterii Resin Extract, Calendula Officinalis Extract, Camellia Sinensis Leaf Extract, Camphor, Carbomer, Glycerin, Ilex Paraguariensis Leaf Extract, Isopropyl Alcohol, Isopropyl Myristate, Melissa Officinalis (Lemon Balm) Leaf Extract, Silica, Tocopheryl Acetate, Water, Yllow 5.

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 temporarily relief of minor aches and pains of muscles and joints associated with arthritis, simple backache, strains and sprains

Purpose

Information about the drug product’s indications for use.
Purpose Pain Relieving Gel

Spl product data elements

Usually a list of ingredients in a drug product.
Target Up and Up Pain Relief Menthol Topical Analgesic Roll-On MENTHOL ALOE VERA LEAF ARCTIUM LAPPA ROOT ARNICA MONTANA FLOWER FRANKINCENSE CALENDULA OFFICINALIS FLOWER GREEN TEA LEAF CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) GLYCERIN ILEX PARAGUARIENSIS LEAF ISOPROPYL ALCOHOL ISOPROPYL MYRISTATE MELISSA OFFICINALIS LEAF SILICON DIOXIDE .ALPHA.-TOCOPHEROL ACETATE FD&C BLUE NO. 1 WATER MENTHOL, UNSPECIFIED FORM MENTHOL, UNSPECIFIED FORM CAMPHOR (SYNTHETIC) AMINOMETHYLPROPANOL FD&C YELLOW NO. 5

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 82937E

Ask doctor

Information about when a doctor should be consulted about existing conditions or sumptoms before using the drug product, including all warnings for persons with certain preexisting conditions (excluding pregnancy) and all warnings for persons experiencing certain symptoms. The warnings under this heading are those intended only for situations in which consumers should not use the product until a doctor is consulted.
Ask a doctor before use if you have sensitive skin

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 on wounds or damaged skin on irritated skin with other ointments, creams, sprays, or liniments

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 symptoms 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 or on mucous membranes do not bandage tightly do not use with heating pad or device

Pregnancy or breast feeding

Pregnancy or Breast feeding
If pregnant or breast-feeding, ask a health professional before use.

Storage and handling

Information about safe storage and handling of the drug product.
Other information Store in a cool dry place

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. Flammable: Keep away from excessive heat or open flame

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