NDC 12022-009

Glovers Anti-Dandruff

Sulfur, Salicylic Acid

Glovers Anti-Dandruff is a Topical Ointment in the Human Otc Drug category. It is labeled and distributed by J. Strickland & Co.. The primary component is Sulfur; Salicylic Acid.

Product ID12022-009_7aa3171b-3717-48d6-e053-2991aa0a6aec
NDC12022-009
Product TypeHuman Otc Drug
Proprietary NameGlovers Anti-Dandruff
Generic NameSulfur, Salicylic Acid
Dosage FormOintment
Route of AdministrationTOPICAL
Marketing Start Date2001-09-20
Marketing CategoryOTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
Application Numberpart358H
Labeler NameJ. Strickland & Co.
Substance NameSULFUR; SALICYLIC ACID
Active Ingredient Strength50 mg/g; mg/g
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 12022-009-00

28 g in 1 JAR (12022-009-00)
Marketing Start Date2001-09-20
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 12022-009-00 [12022000900]

Glovers Anti-Dandruff OINTMENT
Marketing CategoryOTC monograph final
Application Numberpart358H
Product TypeHUMAN OTC DRUG
Marketing Start Date2001-09-20

NDC 12022-009-01 [12022000901]

Glovers Anti-Dandruff OINTMENT
Marketing CategoryOTC monograph final
Application Numberpart358H
Product TypeHUMAN OTC DRUG
Marketing Start Date2001-09-20

Drug Details

Active Ingredients

IngredientStrength
SULFUR50 mg/g

OpenFDA Data

SPL SET ID:49fd4e03-736c-429a-8972-7302b732f816
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 247682
  • NDC Crossover Matching brand name "Glovers Anti-Dandruff" or generic name "Sulfur, Salicylic Acid"

    NDCBrand NameGeneric Name
    12022-009Glovers Anti-DandruffSulfur, Salicylic Acid
    61995-0030J1003005 Jason Dandruff ReliefSulfur, Salicylic Acid
    61995-0302Jason Dandruff Relief TreatmentSulfur, Salicylic Acid
    72317-001RosaAcne ReliefSulfur, Salicylic Acid
    12022-035Sulfur 8 Scalp Therapy Medicated Dandruff Control Scalp Butter CreamSULFUR, SALICYLIC ACID

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