51706-961 NDC - CRAZY CLEANZ HAND SANITIZER BERRY SWIRL SCENTED ()

Drug Information

  • Product NDC: 51706-961
  • Proprietary Name: Crazy Cleanz Hand Sanitizer Berry Swirl Scented
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Landy International
Product Type:
FDA Application Number: M003
Marketing Category: OTC MONOGRAPH DRUG
Start Marketing Date:10/30/2020
End Marketing Date:10/6/2024

Package Information

No. Package Code Package Description Billing Unit
151706-961-01250 mL in 1 BOTTLE (51706-961-01)

NDC Record

Field Name Field Value Definition
PRODUCT NDC51706-961The 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 NAMECrazy Cleanz Hand Sanitizer Berry Swirl ScentedThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE10/30/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
END MARKETING DATE10/6/2024The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
MARKETING CATEGORY NAMEOTC MONOGRAPH DRUGThis is the date that the labeler indicates was the start of its marketing of the drug product.
APPLICATION NUMBERM003Product 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 NAMELandy InternationalThis 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.

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

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