Premjact Male Desensitizer description, usages, side effects, indications, overdosage, supplying and lots more!

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Premjact Male Desensitizer

Pound International
FLEET LABORATORIES LTD

Premjact Male Genital Desensitizer Spray




FULL PRESCRIBING INFORMATION

Active ingredient

Active Ingredient                                                                        Purpose

Lidocaine Base USP 9.6% w/w (approximately 10 mg per spray)    Topical Analgesic

Purpose

Use temporarily reduces sensitivity of the penis, which helps to delay ejaculation in cases of over-rapid or premature ejaculation (coming to a climax too quickly

Keep out of reach of children

Uses

Stop use and consult a doctor

  • if you or your partner develop a rash or irritation, such as burning or itching
  • If you do feel unwell or have any unpleasant effects after using the spray
  • if this product, used as directed, does not provide relief. Premature ejaculation may be due to a condition requiring medical supervision.

Warnings

For external use only

Allergy alert: do not use this product if you or your partner are allergic (sensitive) to local anesthetics

Do not use

  • on broken or inflamed skin
  • if your partner is pregnant

Ask a doctor before use if you have, or ever had, liver or kidney problems

Ask a doctor or pharmacist before use if you are already taking prescribed drugs

When using this product

  • do not get into eyes
  • do not inhale
  • do not exceed a maximum of 24 sprays in 24 hours

directions

  • Apply 3 or more sprays, not to exceed 10, to the head and shaft of the penis before intercourse or use as directed by a doctor
  • Wash product off after intercourse
  • correct quantity and time of application will be determined by individual requirements and you should always use the minimum effective quantity

There are no inactive ingredients

Premjact Male Desensitizer

Premjact Male Desensitizer

Premjact

Male Genital Desensitizer Spray

7/16 Fl.Oz.

Premjact Male Desensitizer

Lidocaine SPRAY, METERED

Product Information

Product Type Human otc drug label Item Code (Source) NDC:57707-058
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
LIDOCAINE LIDOCAINE 9.6 g

Inactive Ingredients

Ingredient Name Strength
ISOPROPYL MYRISTATE
STEARIC ACID

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:57707-058-01 12 in 1 CAN
2 NDC:57707-058-02 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part348 2013-05-09


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Be sure to consult your doctor before taking any medication!
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