41163-943 NDC - SUPERVALUE EQUALINE SPORT SPF 50 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE)

Drug Information

Product NDC: 41163-943

Proprietary Name: Supervalue Equaline Sport SPF 50

Non Proprietary Name: Avobenzone, Homosalate, Octisalate, Octocrylene, Oxybenzone

Active Ingredient(s):
  • 30 mg/g AVOBENZONE;
  • 100 mg/g HOMOSALATE;
  • 50 mg/g OCTISALATE;
  • 40 mg/g OCTOCRYLENE;
  • 50 mg/g OXYBENZONE


Administration Route(s): TOPICAL

Dosage Form(s): SPRAY

Labeler Information

Labeler Name: SUPERVALU INC.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date:1/10/2014

Package Information

No. Package Code Package Description Billing Unit
141163-943-64414 CAN in 1 PACKAGE (41163-943-64) / 207 g in 1 CAN (41163-943-86)

NDC Record

Field Name Field Value Definition
PRODUCT NDC41163-943The 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.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates 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 NAMESupervalue Equaline Sport SPF 50The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEAvobenzone, Homosalate, Octisalate, Octocrylene, OxybenzoneThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMESPRAYThe translation of the dosage form Code submitted by the firm.
ROUTE NAMETOPICALThe 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.
START MARKETING DATE1/10/2014This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEOTC MONOGRAPH NOT FINALProduct 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.
APPLICATION NUMBERpart352The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
LABELER NAMESUPERVALU INC.The translation of the dosage form Code submitted by the firm.
SUBSTANCE NAMEAVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONEThe translation of the route code submitted by the firm, indicating route of administration.
ACTIVE NUMERATOR STRENGTH30; 100; 50; 40; 50This is the date that the labeler indicates was the start of its marketing of the drug product.
ACTIVE INGRED UNITmg/g; mg/g; mg/g; mg/g; mg/g 

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This page was last updated on: 4/12/2024