NDC 58593-782

Finafta MultiOral

Benzocaine

Finafta MultiOral is a Oral Spray in the Human Otc Drug category. It is labeled and distributed by Efficient Laboratories Inc.. The primary component is Benzocaine.

• Product ID: 58593-782_60c818cd-e3ee-4248-a867-c708c7b010a7
• NDC: 58593-782
• Product Type: Human Otc Drug
• Proprietary Name: Finafta MultiOral
• Generic Name: Benzocaine
• Dosage Form: Spray
• Route of Administration: ORAL
• Marketing Start Date: 2004-09-01
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part356
• Labeler Name: Efficient Laboratories Inc.
• Substance Name: BENZOCAINE
• Active Ingredient Strength: 8 mg/100mL
• NDC Exclude Flag: N
• Listing Certified Through: 2021-12-31

Packaging

NDC 58593-782-02

1 BOTTLE, SPRAY in 1 CARTON (58593-782-02) > 59 mL in 1 BOTTLE, SPRAY

• Marketing Start Date: 2004-09-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 58593-782-02 [58593078202]

Finafta MultiOral SPRAY

• Marketing Category: OTC monograph not final
• Application Number: part356
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2004-09-01
• Inactivation Date: 2020-01-31
• Reactivation Date: 2020-02-19

Drug Details

Active Ingredients

Ingredient	Strength
BENZOCAINE	7.5 mg/100mL

OpenFDA Data

• SPL SET ID: 28c5a993-fb5f-4091-af15-32ccae4b9a7d
• Manufacturer:
  • Efficient Laboratories Inc.
• UNII:
  • U3RSY48JW5
• RxNorm Concept Unique ID - RxCUI:
  • 1110820
  • 1110816
• UPC Code:
  • 0000856147829

NDC Crossover Matching brand name "Finafta MultiOral" or generic name "Benzocaine"

NDC	Brand Name	Generic Name
58593-782	Finafta MultiOral	Finafta MultiOral
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