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Lactigo - Medication Information

Product NDC Code 72481-101
Drug Name

Lactigo

Type Brand
Active Ingredients
Menthol, unspecified form 12.5 mg/ml
Route TOPICAL
Dosage Form GEL
RxCUI drug identifier 866128
Application Number M017
Labeler Name LactiGo, Inc.
Packages
Package NDC Code Description
72481-101-03 100 ml in 1 bottle, pump (72481-101-03)
72481-101-32 946 ml in 1 bottle, pump (72481-101-32)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredient Menthol 1.25%

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. Children under 2 years of age: Consult a doctor.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients Ethoxydiglycol, glycerine, L-carnosine, magnesium sulfate, phenoxyethanol, 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.
Use For the temporary relief of minor aches and pains of muscles and joints.

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.
LactiGo MENTHOL MAGNESIUM SULFATE ANHYDROUS DIETHYLENE GLYCOL MONOETHYL ETHER WATER CARNOSINE XANTHAN GUM PHENOXYETHANOL MENTHOL, UNSPECIFIED FORM MENTHOL, UNSPECIFIED FORM GLYCERIN White to off white

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_100 label_946

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 to avoid accidental ingestion. If swallowed, get medical help or contact a Poison Control Center immediately.

Questions

A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.
Questions? 1-844-522-8446

Storage and handling

Information about safe storage and handling of the drug product.
Other information Store at 15°C to 30°C (59°F to 86°F).

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. Avoid contact with eyes and mucous membranes. If contention worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a doctor. Do not apply to wounds or damaged skin. Do not bandage tightly.

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