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Natures craft lidocaine male genital desensitizer - Medication Information

Product NDC Code 73382-185
Drug Name

Natures craft lidocaine male genital desensitizer

Type Brand
Pharm Class Amide Local Anesthetic [EPC],
Amides [CS],
Antiarrhythmic [EPC],
Local Anesthesia [PE]
Active Ingredients
Lidocaine hydrochloride 10 mg/ml
Route TOPICAL
Dosage Form LIQUID
Application Number M017
Labeler Name Natures Design Products LLC
Packages
Package NDC Code Description
73382-185-01 1 bottle, spray in 1 box (73382-185-01) / 30 ml in 1 bottle, spray
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredient: Lidocaine HCl 10mg/Spray 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 3 or more sprays, not to exceed 10, to head and shaft of penis before intercourse, or use as directed by a doctor. Wash product off after intercourse.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Other Ingredients: Aqua (Deionized Water), Ethylhexylglycerin, Isopropyl Myristate, Parfum (Fragrance), Phenoxyethanol, Polysorbate-20, Stearic Acid.

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.
Indications: For temporary male genital desensitization, helping to slow the onset of ejaculation.

Purpose

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

Spl product data elements

Usually a list of ingredients in a drug product.
NATURES CRAFT LIDOCAINE Male Genital Desensitizer LIDOCAINE HYDROCHLORIDE WATER ETHYLHEXYLGLYCERIN ISOPROPYL MYRISTATE PHENOXYETHANOL POLYSORBATE 20 STEARIC ACID LIDOCAINE HYDROCHLORIDE LIDOCAINE LIDOCAINE

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: Bottle

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: Additional Information: Store at room temperature.

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, consult physician. Premature ejaculation may be due to a condition requiring medical supervision. If this product, when used as directed, does not provide relief, discontinue use and consult a physician. If you or your partner develop a rash or irritation, such as burning or itching, discontinue use. If symptoms persist, consult physician.

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

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