NDC 10129-035

GingiCaine Gel

Gingicaine Gel Banana Flavor

GingiCaine Gel is a Dental; Oral; Periodontal Gel in the Human Otc Drug category. It is labeled and distributed by Gingi-pak A Division Of The Belport. The primary component is Benzocaine.

• Product ID: 10129-035_642d43ac-7fd6-1a7d-e053-2991aa0a951a
• NDC: 10129-035
• Product Type: Human Otc Drug
• Proprietary Name: GingiCaine Gel
• Generic Name: Gingicaine Gel Banana Flavor
• Dosage Form: Gel
• Route of Administration: DENTAL; ORAL; PERIODONTAL
• Marketing Start Date: 1993-07-06
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part356
• Labeler Name: Gingi-Pak a Division of the Belport
• Substance Name: BENZOCAINE
• Active Ingredient Strength: 200 mg/1
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 10129-035-01

1 GEL in 1 BOTTLE, PLASTIC (10129-035-01)

• Marketing Start Date: 2001-05-07
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 10129-035-05 [10129003505]

GingiCaine Gel GEL

• Marketing Category: OTC monograph not final
• Application Number: part356
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 1993-07-06

NDC 10129-035-01 [10129003501]

GingiCaine Gel GEL

• Marketing Category: OTC monograph not final
• Application Number: part356
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2001-05-07

NDC 10129-035-03 [10129003503]

GingiCaine Gel GEL

• Marketing Category: OTC monograph not final
• Application Number: part356
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 1993-07-06

Drug Details

Active Ingredients

Ingredient	Strength
BENZOCAINE	200 mg/1

OpenFDA Data

• SPL SET ID: 62857d06-a829-4efa-e053-2991aa0a6d15
• Manufacturer:
  • Gingi-Pak a Division of the Belport
• UNII:
  • U3RSY48JW5
• RxNorm Concept Unique ID - RxCUI:
  • 238910
  • 543801