30142-901 NDC - KROGER SPORT SUNSCREEN ()

Drug Information

  • Product NDC: 30142-901
  • Proprietary Name: Kroger Sport Sunscreen
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: THE KROGER CO
Product Type:
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date:11/19/2012

Package Information

No. Package Code Package Description Billing Unit
130142-901-2256 g in 1 BOTTLE, PLASTIC (30142-901-22)
230142-901-56226 g in 1 BOTTLE, PLASTIC (30142-901-56)

NDC Record

Field Name Field Value Definition
PRODUCT NDC30142-901The 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 NAMEKroger Sport 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.
PROPRIETARY NAME SUFFIXSPF 30A suffix to the proprietary name, a value here should be appended to the ProprietaryName field to obtain the complete name of the product. This suffix is often used to distinguish characteristics of a product such as extended release (“XR”) or sleep aid (“PM”). Although many companies follow certain naming conventions for suffices, there is no recognized standard.
START MARKETING DATE11/19/2012This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEOTC MONOGRAPH NOT FINALThe translation of the route code submitted by the firm, indicating route of administration.
APPLICATION NUMBERpart352This 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 NAMETHE KROGER COName 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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