NDC 69020-207

MAKESENSE Pain Relief

Benzocaine

MAKESENSE Pain Relief is a Topical Gel in the Human Otc Drug category. It is labeled and distributed by Cherry Hill Sales Co. The primary component is Benzocaine.

• Product ID: 69020-207_dbb2fffb-9c0c-4df5-ac7e-b15a9f83e28a
• NDC: 69020-207
• Product Type: Human Otc Drug
• Proprietary Name: MAKESENSE Pain Relief
• Generic Name: Benzocaine
• Dosage Form: Gel
• Route of Administration: TOPICAL
• Marketing Start Date: 2014-07-15
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part356
• Labeler Name: Cherry Hill Sales Co
• Substance Name: BENZOCAINE
• Active Ingredient Strength: 20 g/100g
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 69020-207-14

14 g in 1 TUBE (69020-207-14)

• Marketing Start Date: 2014-07-15
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 69020-207-14 [69020020714]

MAKESENSE Pain Relief GEL

• Marketing Category: OTC monograph not final
• Application Number: part356
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2014-07-15
• Inactivation Date: 2019-11-27

Drug Details

Active Ingredients

Ingredient	Strength
BENZOCAINE	20 g/100g

OpenFDA Data

• SPL SET ID: 4d553377-efec-4b6d-822c-46c301894d18
• Manufacturer:
  • Cherry Hill Sales Co
• UNII:
  • U3RSY48JW5
• RxNorm Concept Unique ID - RxCUI:
  • 238910

NDC Crossover Matching brand name "MAKESENSE Pain Relief" or generic name "Benzocaine"

NDC	Brand Name	Generic Name
69020-207	MAKESENSE Pain Relief	MAKESENSE Pain Relief
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