NDC 41391-119

Myo-Breathe

Menthol

Myo-Breathe is a Topical Gel in the Human Otc Drug category. It is labeled and distributed by Myo-breathe,llc. The primary component is Menthol.

Product ID41391-119_efeb468c-631c-4c9f-ba4c-7e1576c277c2
NDC41391-119
Product TypeHuman Otc Drug
Proprietary NameMyo-Breathe
Generic NameMenthol
Dosage FormGel
Route of AdministrationTOPICAL
Marketing Start Date2009-01-10
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart348
Labeler NameMyo-Breathe,LLC
Substance NameMENTHOL
Active Ingredient Strength40 mg/mL
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 41391-119-19

473 mL in 1 BOTTLE, PUMP (41391-119-19)
Marketing Start Date2009-01-10
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 41391-119-19 [41391011919]

Myo-Breathe GEL
Marketing CategoryOTC monograph not final
Application Numberpart348
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-07-28
Inactivation Date2020-01-31

NDC 41391-119-12 [41391011912]

Myo-Breathe GEL
Marketing CategoryOTC monograph not final
Application Numberpart348
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-01-10
Inactivation Date2020-01-31

NDC 41391-119-15 [41391011915]

Myo-Breathe GEL
Marketing CategoryOTC monograph not final
Application Numberpart348
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-01-10
Marketing End Date2015-07-28

NDC 41391-119-14 [41391011914]

Myo-Breathe GEL
Marketing CategoryOTC monograph not final
Application Numberpart348
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-01-10
Marketing End Date2015-07-28

NDC 41391-119-11 [41391011911]

Myo-Breathe GEL
Marketing CategoryOTC monograph not final
Application Numberpart348
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-01-10
Inactivation Date2020-01-31

NDC 41391-119-13 [41391011913]

Myo-Breathe GEL
Marketing CategoryOTC monograph not final
Application Numberpart348
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-01-10
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
MENTHOL40 mg/mL

OpenFDA Data

SPL SET ID:40fa3155-b568-4f2a-ad9e-ea18a039d2f8
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 415974
  • NDC Crossover Matching brand name "Myo-Breathe" or generic name "Menthol"

    NDCBrand NameGeneric Name
    41391-119Myo-BreatheMyo-Breathe
    41391-120Myo-BreatheMyo-Breathe
    0363-1071Cherry Cough DropMenthol
    0363-1086Cherry Cough DropsMenthol
    0363-0150Cool n Heat Patch for Arm, Neck and LegMenthol
    0363-0152Cool n Heat Patch for BackMenthol
    0363-1072Honey Lemon Cough DropMenthol
    0363-1087Honey Lemon Cough DropMenthol
    0219-0203Humphreys Bendito Alcoholadomenthol
    0363-1070Menthol Cough Dropmenthol
    0363-1084Menthol Cough Dropmenthol
    0067-2067Mineral IceMenthol
    0316-0226Mineral IceMenthol
    0316-0290Mineral Ice Quick Dry FoamMenthol
    0363-0151Pain Relieving PatchMenthol
    0363-1077SF Honey Lemon Cough DropMenthol
    0363-1085SF Menthol Cough DropMenthol
    0363-0043Studio 35 Medicated BodyMenthol
    0363-0864Walgreens Cold Pain ReliefMENTHOL
    0363-0874Walgreens Cold Pain ReliefMENTHOL
    0363-0966Walgreens Sunburn ReliefMenthol

    Trademark Results [Myo-Breathe]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    MYO-BREATHE
    MYO-BREATHE
    77046052 3315707 Dead/Cancelled
    MYO-BREATHE, LLC
    2006-11-16
    MYO-BREATHE
    MYO-BREATHE
    77046052 3315707 Dead/Cancelled
    Aquilino, Vincent
    2006-11-16

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