74047-001 NDC - ALCOHOL HAND SANITIZER GEL ()

Drug Information

  • Product NDC: 74047-001
  • Proprietary Name: Alcohol Hand Sanitizer Gel
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Shantou Kangjie Daily Chemical Industry Co.,Ltd
Product Type:
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date:4/16/2020
End Marketing Date:6/26/2025

Package Information

No. Package Code Package Description Billing Unit
174047-001-0120 mL in 1 BOTTLE (74047-001-01)
274047-001-0225 mL in 1 BOTTLE (74047-001-02)
374047-001-0330 mL in 1 BOTTLE (74047-001-03)
474047-001-0450 mL in 1 BOTTLE (74047-001-04)
574047-001-0560 mL in 1 BOTTLE (74047-001-05)
674047-001-06100 mL in 1 BOTTLE (74047-001-06)
774047-001-07120 mL in 1 BOTTLE (74047-001-07)
874047-001-08250 mL in 1 BOTTLE (74047-001-08)
974047-001-09300 mL in 1 BOTTLE (74047-001-09)
1074047-001-10500 mL in 1 BOTTLE (74047-001-10)
1174047-001-11800 mL in 1 BOTTLE (74047-001-11)
1274047-001-121000 mL in 1 BOTTLE (74047-001-12)
1374047-001-134000 mL in 1 BOTTLE (74047-001-13)
1474047-001-145000 mL in 1 BOTTLE (74047-001-14)
1574047-001-1525000 mL in 1 BOTTLE (74047-001-15)
1674047-001-1650000 mL in 1 BOTTLE (74047-001-16)

NDC Record

Field Name Field Value Definition
PRODUCT NDC74047-001The 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 NAMEAlcohol Hand Sanitizer GelThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE4/16/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
END MARKETING DATE6/26/2025This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
MARKETING CATEGORY NAMEUNAPPROVED DRUG OTHERProduct 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.
LABELER NAMEShantou Kangjie Daily Chemical Industry Co.,LtdName of Company corresponding to the labeler code segment of the Product NDC.

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

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