NDC 10157-9893

Kank-A with Blistex Medicated Lip

Benzocaine, Dimethicone, Camphor (synthetic), Menthol, Unspecified Form, And Phenol

Kank-A with Blistex Medicated Lip is a Kit in the Human Otc Drug category. It is labeled and distributed by Blistex Inc.. The primary component is .

• Product ID: 10157-9893_52e8f887-4da6-49af-9455-5c56209a1170
• NDC: 10157-9893
• Product Type: Human Otc Drug
• Proprietary Name: Kank-A with Blistex Medicated Lip
• Generic Name: Benzocaine, Dimethicone, Camphor (synthetic), Menthol, Unspecified Form, And Phenol
• Dosage Form: Kit
• Marketing Start Date: 2018-11-19
• Marketing Category: OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
• Application Number: part346
• Labeler Name: Blistex Inc.
• Active Ingredient Strength: 0
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 10157-9893-1

1 KIT in 1 BLISTER PACK (10157-9893-1) * 9.75 mL in 1 BOTTLE, WITH APPLICATOR * 6 g in 1 TUBE

• Marketing Start Date: 2018-11-19
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 10157-9893-1 [10157989301]

Kank-A with Blistex Medicated Lip KIT

• Marketing Category: OTC monograph final
• Application Number: part346
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2018-11-19
• Marketing End Date: 2019-08-08

Drug Details

OpenFDA Data

• SPL SET ID: 976f983a-73d4-4bd8-88e1-08c907fa78a6
• Manufacturer:
  • Blistex Inc.
• RxNorm Concept Unique ID - RxCUI:
  • 308657
  • 2107300
• UPC Code:
  • 0041388203911