33992-8878 NDC - JAPANESE BLOSSOM SCENTED HAND SANITIZER ()

Drug Information

  • Product NDC: 33992-8878
  • Proprietary Name: JAPANESE BLOSSOM SCENTED HAND SANITIZER
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Greenbrier International, Inc.
Product Type:
FDA Application Number: part333E
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date:4/5/2017
End Marketing Date:12/31/2019

Package Information

No. Package Code Package Description Billing Unit
133992-8878-029.6 mL in 1 BOTTLE (33992-8878-0)

NDC Record

Field Name Field Value Definition
PRODUCT NDC33992-8878The 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.
PROPRIETARY NAMEJAPANESE BLOSSOM SCENTED HAND SANITIZERThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE4/5/2017The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
END MARKETING DATE12/31/2019The translation of the dosage form Code submitted by the firm.
MARKETING CATEGORY NAMEOTC MONOGRAPH NOT FINALThe translation of the route code submitted by the firm, indicating route of administration.
APPLICATION NUMBERpart333EThis is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEGreenbrier International, Inc.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.

Download Record

Download this NDC record record in Text format: Export

Download this NDC record record in Excel (CSV) format: Export

Download this NDC record record in XML format: Export

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