37205-723 NDC - LEADER KIDS ()

Drug Information

  • Product NDC: 37205-723
  • Proprietary Name: Leader Kids
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Cardinal Health
Product Type:
FDA Application Number: M020
Marketing Category: OTC MONOGRAPH DRUG
Start Marketing Date:1/15/2012
End Marketing Date:1/26/2020

Package Information

No. Package Code Package Description Billing Unit
137205-723-30177 mL in 1 CAN (37205-723-30)

NDC Record

Field Name Field Value Definition
PRODUCT NDC37205-723The 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 NAMELeader KidsThe 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 NAME SUFFIXSPF 50 SunscreenIndicates 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.
START MARKETING DATE1/15/2012This is the date that the labeler indicates was the start of its marketing of the drug product.
END MARKETING DATE1/26/2020The 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.
MARKETING CATEGORY NAMEOTC MONOGRAPH DRUGThe translation of the dosage form Code submitted by the firm.
APPLICATION NUMBERM020This 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 NAMECardinal HealthName of Company corresponding to the labeler code segment of the Product NDC.

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

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