NDC 10157-9302

Blistex Foille Medicated First Aid

Benzocaine And Chloroxylenol

Blistex Foille Medicated First Aid is a Topical Ointment in the Human Otc Drug category. It is labeled and distributed by Blistex Inc.. The primary component is Benzocaine; Chloroxylenol.

• Product ID: 10157-9302_3722476b-f75e-43af-b09b-afe4c28857fb
• NDC: 10157-9302
• Product Type: Human Otc Drug
• Proprietary Name: Blistex Foille Medicated First Aid
• Generic Name: Benzocaine And Chloroxylenol
• Dosage Form: Ointment
• Route of Administration: TOPICAL
• Marketing Start Date: 2013-03-05
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part348
• Labeler Name: Blistex Inc.
• Substance Name: BENZOCAINE; CHLOROXYLENOL
• Active Ingredient Strength: 5 g/100g; g/100g
• NDC Exclude Flag: N
• Listing Certified Through: 2022-12-31

Packaging

NDC 10157-9302-3

1 TUBE in 1 CARTON (10157-9302-3) > 14 g in 1 TUBE

• Marketing Start Date: 2016-09-23
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 10157-9302-3 [10157930203]

Blistex Foille Medicated First Aid OINTMENT

• Marketing Category: OTC MONOGRAPH NOT FINAL
• Application Number: part348
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2016-09-23

NDC 10157-9302-4 [10157930204]

Blistex Foille Medicated First Aid OINTMENT

• Marketing Category: OTC MONOGRAPH NOT FINAL
• Application Number: part348
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2013-03-05

Drug Details

Active Ingredients

Ingredient	Strength
BENZOCAINE	5 g/100g

OpenFDA Data

• SPL SET ID: e2eca808-e97b-43e0-aa51-7025cc61c7a8
• Manufacturer:
  • Blistex Inc.
• UNII:
  • U3RSY48JW5
  • 0F32U78V2Q
• RxNorm Concept Unique ID - RxCUI:
  • 213034
  • 199005
• UPC Code:
  • 0041388003023