80477-001 NDC - WHITE CLOUD HAND SANITIZER ()

Drug Information

  • Product NDC: 80477-001
  • Proprietary Name: White Cloud Hand Sanitizer
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Moderplas, S. de R.L. de C.V.
Product Type:
FDA Application Number: part333E
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date:9/4/2020
End Marketing Date:12/31/2021

Package Information

No. Package Code Package Description Billing Unit
180477-001-00300 mL in 1 BOTTLE (80477-001-00)

NDC Record

Field Name Field Value Definition
PRODUCT NDC80477-001Indicates 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 NAMEWhite Cloud Hand SanitizerThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
START MARKETING DATE9/4/2020The translation of the dosage form Code submitted by the firm.
END MARKETING DATE12/31/2021This 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 NAMEOTC MONOGRAPH NOT FINALThis is the date that the labeler indicates was the start of its marketing of the drug product.
APPLICATION NUMBERpart333EName of Company corresponding to the labeler code segment of the Product NDC.
LABELER NAMEModerplas, S. de R.L. de C.V.An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

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

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