69423-661 NDC - OLD SPICE VISTA VERDE (ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY)

Drug Information

  • Product NDC: 69423-661
  • Proprietary Name: Old Spice Vista Verde
  • Non Proprietary Name: Aluminum Zirconium Tetrachlorohydrex Gly
  • Active Ingredient(s): 15 g/100g ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
  • Administration Route(s): TOPICAL
  • Dosage Form(s): STICK

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:8/1/2022

Package Information

No. Package Code Package Description Billing Unit
169423-661-7373 g in 1 CYLINDER (69423-661-73)

NDC Record

Field Name Field Value Definition
PRODUCT NDC69423-661The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN OTC DRUGThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
PROPRIETARY NAMEOld Spice Vista VerdeThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEAluminum Zirconium Tetrachlorohydrex GlyThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMESTICKThe 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 DATE8/1/2022Product 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.
MARKETING CATEGORY NAMEOTC MONOGRAPH DRUGThis 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.
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 CompanyThis 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.
SUBSTANCE NAMEALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLYThe translation of the route code submitted by the firm, indicating route of administration.
ACTIVE NUMERATOR STRENGTH15 
ACTIVE INGRED UNITg/100g 

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This page was last updated on: 11/21/2025

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