69423-704 NDC - SECRET CLINICAL FREE AND SENSITIVE SOFT (ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY)

Drug Information

  • Product NDC: 69423-704
  • Proprietary Name: Secret Clinical Free and Sensitive Soft
  • Non Proprietary Name: Aluminum Zirconium Trichlorohydrex Gly
  • Active Ingredient(s): 20 g/100g ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY
  • Administration Route(s): TOPICAL
  • Dosage Form(s): CREAM

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:3/1/2023

Package Information

No. Package Code Package Description Billing Unit
169423-704-451 CYLINDER in 1 CARTON (69423-704-45) / 45 g in 1 CYLINDER

NDC Record

Field Name Field Value Definition
PRODUCT NDC69423-704The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
PRODUCT TYPE NAMEHUMAN OTC DRUGA suffix to the proprietary name, a value here should be appended to the ProprietaryName field to obtain the complete name of the product. This suffix is often used to distinguish characteristics of a product such as extended release (“XR”) or sleep aid (“PM”). Although many companies follow certain naming conventions for suffices, there is no recognized standard.
PROPRIETARY NAMESecret Clinical Free and Sensitive SoftThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
NON PROPRIETARY NAMEAluminum Zirconium Trichlorohydrex GlyThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMECREAMThe translation of the dosage form Code submitted by the firm.
ROUTE NAMETOPICALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE3/1/2023This 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 Company 
SUBSTANCE NAMEALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY 
ACTIVE NUMERATOR STRENGTH20 
ACTIVE INGRED UNITg/100g 

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

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