75439-002 NDC - INSTANT HAND SANITIZER ()

Drug Information

  • Product NDC: 75439-002
  • Proprietary Name: Instant Hand Sanitizer
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Guangzhou Yucaitang Cosmetics Co., Ltd
Product Type:
FDA Application Number: part333A
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date:5/14/2020

Package Information

No. Package Code Package Description Billing Unit
175439-002-015 mL in 1 BAG (75439-002-01)
275439-002-0229 mL in 1 AMPULE (75439-002-02)
375439-002-0330 mL in 1 AMPULE (75439-002-03)
475439-002-0450 mL in 1 BOTTLE (75439-002-04)
575439-002-0559 mL in 1 AMPULE (75439-002-05)
675439-002-0660 mL in 1 BOTTLE (75439-002-06)
775439-002-07100 mL in 1 BOTTLE (75439-002-07)
875439-002-08200 mL in 1 BOTTLE (75439-002-08)
975439-002-09238 mL in 1 BOTTLE (75439-002-09)
1075439-002-10250 mL in 1 BOTTLE (75439-002-10)
1175439-002-11260 mL in 1 BOTTLE (75439-002-11)
1275439-002-12300 mL in 1 BOTTLE (75439-002-12)
1375439-002-13400 mL in 1 BOTTLE (75439-002-13)
1475439-002-14500 mL in 1 BOTTLE (75439-002-14)
1575439-002-15750 mL in 1 BOTTLE (75439-002-15)
1675439-002-161000 mL in 1 BOTTLE (75439-002-16)
1775439-002-171250 mL in 1 BOTTLE (75439-002-17)
1875439-002-182000 mL in 1 BOTTLE (75439-002-18)
1975439-002-195000 mL in 1 BOTTLE (75439-002-19)

NDC Record

Field Name Field Value Definition
PRODUCT NDC75439-002The 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 NAMEInstant 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 DATE5/14/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEOTC MONOGRAPH NOT 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 NUMBERpart333AThis 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 NAMEGuangzhou Yucaitang Cosmetics Co., LtdName 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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