NDC 70742-089

PROLONG

Benzocaine

PROLONG is a Topical Gel in the Human Otc Drug category. It is labeled and distributed by Product Max Group Inc. The primary component is Benzocaine.

• Product ID: 70742-089_0e144306-e60f-4de8-a6cb-70882bd85db8
• NDC: 70742-089
• Product Type: Human Otc Drug
• Proprietary Name: PROLONG
• Generic Name: Benzocaine
• Dosage Form: Gel
• Route of Administration: TOPICAL
• Marketing Start Date: 2016-06-15
• Marketing Category: OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
• Application Number: part348
• Labeler Name: Product Max Group Inc
• Substance Name: BENZOCAINE
• Active Ingredient Strength: 2833 mg/60mL
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 70742-089-01

60 mL in 1 BOTTLE (70742-089-01)

• Marketing Start Date: 2016-06-15
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 70742-089-01 [70742008901]

PROLONG GEL

• Marketing Category: OTC monograph final
• Application Number: part348
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2016-06-15
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
BENZOCAINE	2833 mg/60mL

OpenFDA Data

• SPL SET ID: 014000ad-2500-44ee-b593-6f5fe189757e
• Manufacturer:
  • Product Max Group Inc
• UNII:
  • U3RSY48JW5

NDC Crossover Matching brand name "PROLONG" or generic name "Benzocaine"

NDC	Brand Name	Generic Name
70742-089	PROLONG	PROLONG
0283-0220	HurriCaine	Benzocaine
0283-0293	HurriCaine	Benzocaine
0283-0520	HurriCaine	Benzocaine
0283-0569	HurriCaine	Benzocaine
0283-0679	HurriCaine	Benzocaine
0283-0871	HurriCaine	BENZOCAINE
0283-0886	HurriCaine	Benzocaine
0283-0914	HurriCaine	Benzocaine
0283-0920	HurriCaine	Benzocaine
0283-0998	HurriCaine	Benzocaine
0283-1016	HurriCaine	BENZOCAINE