75742-043 NDC - ASHLEYBELLE MOISTURIZING HAND SANITIZER SUNFLOWER HAZE (ETHYL ALCOHOL 70%)

Drug Information

  • Product NDC: 75742-043
  • Proprietary Name: AshleyBelle Moisturizing Hand Sanitizer Sunflower Haze
  • Non Proprietary Name: Ethyl Alcohol 70%
  • Active Ingredient(s): 70 mL/100mL ALCOHOL
  • Administration Route(s): TOPICAL
  • Dosage Form(s): SPRAY

Labeler Information

Field Name Field Value
Labeler Name: Zhejiang Guoyao Jingyue Aerosol Co., Ltd.
Product Type: HUMAN OTC DRUG
FDA Application Number: M003
Marketing Category: OTC MONOGRAPH DRUG
Start Marketing Date:6/4/2025

Package Information

No. Package Code Package Description Billing Unit
175742-043-0129.5 mL in 1 BOTTLE, SPRAY (75742-043-01)

NDC Record

Field Name Field Value Definition
PRODUCT NDC75742-043The 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 DRUGIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAMEAshleyBelle Moisturizing Hand Sanitizer Sunflower HazeThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEEthyl Alcohol 70%Product 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.
DOSAGE FORM NAMESPRAYThis 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.
ROUTE NAMETOPICALName of Company corresponding to the labeler code segment of the Product NDC.
START MARKETING DATE6/4/2025The 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.
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 NUMBERM003This 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 NAMEZhejiang Guoyao Jingyue Aerosol Co., Ltd.Product 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.
SUBSTANCE NAMEALCOHOLThis 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.
ACTIVE NUMERATOR STRENGTH70Name of Company corresponding to the labeler code segment of the Product NDC.
ACTIVE INGRED UNITmL/100mL 

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This page was last updated on: 12/19/2025

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