59535-7901 NDC - JASMINE 3D WHIPPING ESSENCE ()

Drug Information

  • Product NDC: 59535-7901
  • Proprietary Name: Jasmine 3D Whipping Essence
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: AMI Cosmetic Co.,Ltd.
Product Type:
FDA Application Number: part347
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date:4/14/2014
End Marketing Date:1/15/2019

Package Information

No. Package Code Package Description Billing Unit
159535-7901-130 mL in 1 BOTTLE (59535-7901-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC59535-7901This 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.
PROPRIETARY NAMEJasmine 3D Whipping EssenceThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE4/14/2014This is the date that the labeler indicates was the start of its marketing of the drug product.
END MARKETING DATE1/15/2019Product 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 FINALProduct 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 NUMBERpart347This 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 NAMEAMI Cosmetic Co.,Ltd.Name of Company corresponding to the labeler code segment of the Product NDC.

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

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