NDC 71814-410

Aftertest Pain Relief

Benzocaine

Aftertest Pain Relief is a Topical Stick in the Human Otc Drug category. It is labeled and distributed by Diabetic Supply Of Suncoast, Inc.. The primary component is Benzocaine.

• Product ID: 71814-410_79c51ea7-91c4-4ffa-be7c-6961d8958fa0
• NDC: 71814-410
• Product Type: Human Otc Drug
• Proprietary Name: Aftertest Pain Relief
• Generic Name: Benzocaine
• Dosage Form: Stick
• Route of Administration: TOPICAL
• Marketing Start Date: 2017-01-28
• Marketing Category: OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
• Application Number: part348
• Labeler Name: Diabetic Supply of Suncoast, Inc.
• Substance Name: BENZOCAINE
• Active Ingredient Strength: 100 mg/mL
• NDC Exclude Flag: E
• Listing Certified Through: 2018-12-31

Packaging

NDC 71814-410-01

1 APPLICATOR in 1 CARTON (71814-410-01) > 4 mL in 1 APPLICATOR

• Marketing Start Date: 2017-01-28
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 71814-410-01 [71814041001]

Aftertest Pain Relief STICK

• Marketing Category: OTC MONOGRAPH FINAL
• Application Number: part348
• Product Type: HUMAN OTC DRUG
• Billing Unit: ML
• Marketing Start Date: 2017-01-28
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
BENZOCAINE	100 mg/mL

OpenFDA Data

• SPL SET ID: 1469366a-5e93-4a2c-96b6-425b1cc7b2d9
• Manufacturer:
  • Diabetic Supply of Suncoast, Inc.
• UNII:
  • U3RSY48JW5
• RxNorm Concept Unique ID - RxCUI:
  • 245647

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

NDC	Brand Name	Generic Name
71814-410	Aftertest Pain Relief	Aftertest 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