84126-031 NDC - SECRET OUTLAST HYGIENIC FRESH CLEAR (ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY)

Drug Information

  • Product NDC: 84126-031
  • Proprietary Name: Secret Outlast Hygienic Fresh Clear
  • Non Proprietary Name: Aluminum Zirconium Octachlorohydrex Gly
  • Active Ingredient(s): 16 g/100g ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY
  • Administration Route(s): TOPICAL
  • Dosage Form(s): GEL

Labeler Information

Field Name Field Value
Labeler Name: The Procter & Gamble Manufacturing Company
Product Type: HUMAN OTC DRUG
FDA Application Number: M019
Marketing Category: OTC MONOGRAPH DRUG
Start Marketing Date:1/1/2024

Package Information

No. Package Code Package Description Billing Unit
184126-031-7373 g in 1 CYLINDER (84126-031-73)

NDC Record

Field Name Field Value Definition
PRODUCT NDC84126-031This is the date that the labeler indicates was the start of its marketing of the drug product.
PRODUCT TYPE NAMEHUMAN OTC DRUGProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
PROPRIETARY NAMESecret Outlast Hygienic Fresh ClearThis corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
NON PROPRIETARY NAMEAluminum Zirconium Octachlorohydrex Gly 
DOSAGE FORM NAMEGEL 
ROUTE NAMETOPICAL 
START MARKETING DATE1/1/2024This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEOTC MONOGRAPH DRUGProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
APPLICATION NUMBERM019This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
LABELER NAMEThe Procter & Gamble Manufacturing CompanyName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLYAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH16 
ACTIVE INGRED UNITg/100g 

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This page was last updated on: 12/6/2025

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