NDC 10157-9951

Blistex Medicated

Dimethicone, Camphor (synthetic), Menthol, And Phenol

Blistex Medicated is a Topical Ointment in the Human Otc Drug category. It is labeled and distributed by Blistex Inc.. The primary component is Dimethicone; Camphor (synthetic); Menthol, Unspecified Form; Phenol.

Product ID10157-9951_54868a5a-66c4-4a3f-afa5-a80fd3c236c9
NDC10157-9951
Product TypeHuman Otc Drug
Proprietary NameBlistex Medicated
Generic NameDimethicone, Camphor (synthetic), Menthol, And Phenol
Dosage FormOintment
Route of AdministrationTOPICAL
Marketing Start Date2000-12-01
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart348
Labeler NameBlistex Inc.
Substance NameDIMETHICONE; CAMPHOR (SYNTHETIC); MENTHOL, UNSPECIFIED FORM; PHENOL
Active Ingredient Strength1 g/100g; g/100g; g/100g; g/100g
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 10157-9951-1

6 g in 1 TUBE (10157-9951-1)
Marketing Start Date2000-12-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 10157-9951-1 [10157995101]

Blistex Medicated OINTMENT
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart348
Product TypeHUMAN OTC DRUG
Marketing Start Date2000-12-01

NDC 10157-9951-6 [10157995106]

Blistex Medicated OINTMENT
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart348
Product TypeHUMAN OTC DRUG
Marketing Start Date2000-12-01

NDC 10157-9951-2 [10157995102]

Blistex Medicated OINTMENT
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart348
Product TypeHUMAN OTC DRUG
Billing UnitGM
Marketing Start Date2000-12-01

NDC 10157-9951-3 [10157995103]

Blistex Medicated OINTMENT
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart348
Product TypeHUMAN OTC DRUG
Billing UnitGM
Marketing Start Date2000-12-01

NDC 10157-9951-4 [10157995104]

Blistex Medicated OINTMENT
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart348
Product TypeHUMAN OTC DRUG
Marketing Start Date2000-12-01

NDC 10157-9951-8 [10157995108]

Blistex Medicated OINTMENT
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart348
Product TypeHUMAN OTC DRUG
Marketing Start Date2000-12-01

NDC 10157-9951-5 [10157995105]

Blistex Medicated OINTMENT
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart348
Product TypeHUMAN OTC DRUG
Marketing Start Date2000-12-01

NDC 10157-9951-7 [10157995107]

Blistex Medicated OINTMENT
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart348
Product TypeHUMAN OTC DRUG
Marketing Start Date2000-12-01

Drug Details

Active Ingredients

IngredientStrength
DIMETHICONE1.1 g/100g

OpenFDA Data

SPL SET ID:e95439d3-f12b-4c1c-999a-79f2ddba4cfb
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1358991
  • 1358989
  • UPC Code
  • 0041388210209

  • Trademark Results [Blistex]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    BLISTEX
    BLISTEX
    88143446 5924118 Live/Registered
    Blistex Inc.
    2018-10-04
    BLISTEX
    BLISTEX
    78233453 2817472 Live/Registered
    BLISTEX INC.
    2003-04-03
    BLISTEX
    BLISTEX
    74421493 1897266 Dead/Cancelled
    Blistex Bracken Limited Partnership
    1993-08-04
    BLISTEX
    BLISTEX
    73541344 1373396 Live/Registered
    BLISTEX BRACKEN LIMITED PARTNERSHIP
    1985-06-05
    BLISTEX
    BLISTEX
    73136745 1094204 Live/Registered
    BRACKEN, JIM L.
    1977-08-08
    BLISTEX
    BLISTEX
    72226892 0804558 Live/Registered
    BLISTEX COMPANY
    1965-09-01

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.