NDC 58593-781

Finafta Baby

Benzocaine

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

• Product ID: 58593-781_b5686d5b-ca50-4291-8d4e-b34e7db17753
• NDC: 58593-781
• Product Type: Human Otc Drug
• Proprietary Name: Finafta Baby
• Generic Name: Benzocaine
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2000-01-01
• 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/100mg
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 58593-781-02

7100 mg in 1 TUBE (58593-781-02)

• Marketing Start Date: 2000-01-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 58593-781-02 [58593078102]

Finafta Baby LIQUID

• Marketing Category: OTC monograph not final
• Application Number: part356
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2000-01-01

Drug Details

Active Ingredients

Ingredient	Strength
BENZOCAINE	7.5 mg/100mg

OpenFDA Data

• SPL SET ID: 404d36c3-19a4-4fe9-803d-db9b910c0652
• Manufacturer:
  • Efficient Laboratories Inc.
• UNII:
  • U3RSY48JW5
• RxNorm Concept Unique ID - RxCUI:
  • 1092552
  • 199645
• UPC Code:
  • 0000856147812

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

NDC	Brand Name	Generic Name
58593-781	Finafta Baby	Finafta Baby
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