NDC 70742-089 Prolong

NDC Product Code 70742-089

NDC 70742-089-01

Package Description: 60 mL in 1 BOTTLE

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Prolong with NDC 70742-089 is a product labeled by Product Max Group Inc. The generic name of Prolong is . The product's dosage form is and is administered via form.

Labeler Name: Product Max Group Inc

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • HYDROXYETHYL CELLULOSE (140 MPA.S AT 5%) (UNII: 8136Y38GY5)
  • METHYLPARABEN (UNII: A2I8C7HI9T)
  • POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • PROPYLPARABEN (UNII: Z8IX2SC1OH)
  • WATER (UNII: 059QF0KO0R)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Product Max Group Inc
Labeler Code: 70742
Start Marketing Date: 06-15-2016 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2017 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: I - INACTIVATED, the listing data was inactivated by the FDA. What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

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Prolong Product Label Images

Prolong Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Drug Factsactive Ingredient

Benzocaine 5%

Purpose

Male Genital Desensitizer

Keep Out Of Reach Of Children

Keep out of reach of children.If swallowed get medical help or contact a Poison Control Center right away.

Uses

  • Helps in the prevention of premature ejaculation.

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.

Directions

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

Other Information

Do not use if safety seal under cap is broken or missing.

Inactive Ingredients

Hydroxyethylcellulose, Methylparaben, PEG-8, Propylene Glycol, Propylparaben, Water

Prolong Product Label

Www.bodyactionproducts.comDistributed by:Body Action ProductsLutz, FL 33559ACTION BODY PRODUCTSBenzocaine Male Genital DesensitizerPROLONG FOR MENHelps Prolong Sexual PleasureLubricating Gel2 FL OZ (60 ml)

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