58411-254 NDC - SHISEIDO ULTIMATE SUN PROTECTION (OCTINOXATE, OCTOCRYLENE, TITANIUM DIOXIDE, AND ZINC OXIDE)

Drug Information

Product NDC: 58411-254

Proprietary Name: SHISEIDO ULTIMATE SUN PROTECTION

Non Proprietary Name: OCTINOXATE, OCTOCRYLENE, TITANIUM DIOXIDE, and ZINC OXIDE

Active Ingredient(s):
  • 4255 mg/50mL OCTINOXATE;
  • 1725 mg/50mL OCTOCRYLENE;
  • 805 mg/50mL TITANIUM DIOXIDE;
  • 9430 mg/50mL ZINC OXIDE


Administration Route(s): TOPICAL

Dosage Form(s): CREAM

Labeler Information

Labeler Name: SHISEIDO AMERICAS CORPORATION
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date:2/1/2015

Package Information

No. Package Code Package Description Billing Unit
158411-254-601 TUBE in 1 CARTON (58411-254-60) > 50 mL in 1 TUBE
258411-254-611 TUBE in 1 CARTON (58411-254-61) > 30 mL in 1 TUBE
358411-254-621 TUBE in 1 CARTON (58411-254-62) > 15 mL in 1 TUBE

NDC Record

Field Name Field Value Definition
PRODUCT NDC58411-254The 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 NAMESHISEIDO ULTIMATE SUN PROTECTIONThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEOCTINOXATE, OCTOCRYLENE, TITANIUM DIOXIDE, and ZINC OXIDEThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMECREAMThe translation of the dosage form Code submitted by the firm.
ROUTE NAMETOPICALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE2/1/2015This 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 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 NAMESHISEIDO AMERICAS CORPORATIONName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEOCTINOXATE; OCTOCRYLENE; TITANIUM DIOXIDE; ZINC OXIDEThis is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH4255; 1725; 805; 9430 
ACTIVE INGRED UNITmg/50mL; mg/50mL; mg/50mL; mg/50mL 

Download Record

Download this NDC record in Text format: Export

Download this NDC record in Excel (CSV) format: Export

Download this NDC record in XML format: Export

This page was last updated on: 7/3/2020