NDC 72625-130

Ultra Vedic

Feminine Pain Relief

Ultra Vedic is a Topical Patch in the Human Otc Drug category. It is labeled and distributed by Pharmaneek, Inc.. The primary component is Menthol.

Product ID72625-130_1e85f653-754a-4195-9fd3-49456bee4dc7
NDC72625-130
Product TypeHuman Otc Drug
Proprietary NameUltra Vedic
Generic NameFeminine Pain Relief
Dosage FormPatch
Route of AdministrationTOPICAL
Marketing Start Date2019-03-01
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart348
Labeler NamePharmaneek, Inc.
Substance NameMENTHOL
Active Ingredient Strength200 mg/1
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 72625-130-05

1 CARTON in 1 PATCH (72625-130-05) > 5 PATCH in 1 CARTON
Marketing Start Date2019-03-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 72625-130-05 [72625013005]

Ultra Vedic PATCH
Marketing CategoryOTC monograph not final
Application Numberpart348
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-03-01

Drug Details

Active Ingredients

IngredientStrength
MENTHOL200 mg/1

OpenFDA Data

SPL SET ID:86d0da3e-b83f-4829-9a9d-5903cb388d1e
Manufacturer
UNII
UPC Code
  • 0691039063076
  • NDC Crossover Matching brand name "Ultra Vedic" or generic name "Feminine Pain Relief"

    NDCBrand NameGeneric Name
    72625-130Ultra VedicFeminine Pain Relief
    72625-135Ultra VedicPain Relief

    Trademark Results [Ultra Vedic]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    ULTRA VEDIC
    ULTRA VEDIC
    88471902 5949240 Live/Registered
    Ultravedic Inc.
    2019-06-13

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