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Higher control male climax control lubricating - Medication Information

Product NDC Code 70742-180
Drug Name

Higher control male climax control lubricating

Type Brand
Pharm Class Allergens [CS],
Cell-mediated Immunity [PE],
Increased Histamine Release [PE],
Standardized Chemical Allergen [EPC]
Active Ingredients
Benzocaine 50 mg/ml
Route TOPICAL
Dosage Form GEL
Application Number M017
Labeler Name Product Max Group Inc
Packages
Package NDC Code Description
70742-180-02 60 ml in 1 bottle (70742-180-02)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredient Benzocaine 5% Purpose Male Genital Desensitizer

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 Apply a small amount to head and shaft of penis before intercourse. Wash product off after intercourse.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredients Cannabis Sativa (Hemp) Seed Oil, Hydroxyethylcellulose, Methylparaben, PEG-8, Polysorbate 20, Propylene Glycol, Propylparaben, 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 Helps in the prevention of premature ejaculation.

Purpose

Information about the drug product’s indications for use.
Purpose Male Genital Desensitizer

Spl product data elements

Usually a list of ingredients in a drug product.
HIGHER CONTROL Male Climax Control Lubricating BENZOCAINE CANNABIS SATIVA SEED OIL METHYLPARABEN POLYETHYLENE GLYCOL 400 POLYSORBATE 20 PROPYLENE GLYCOL PROPYLPARABEN WATER BENZOCAINE BENZOCAINE

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: 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 Other Information Do not use if safety seal on bottle is broken or missing.

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.

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 the eyes. Premature ejaculation may be due to a condition requiring medical supervision. If this product, used as directed, does not provide relief, discontinue use and consult a doctor. If you or your partner develop a rash or irritation, such as burning or itching, discontinue use. If symptoms persist, consult a doctor. Keep out of reach of children. If swallowed get medical help or contact a 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