58411-359 : Shiseido Ultimate Sun Protection Topical Cream


NDC: 58411-359
Labeler: Shiseido Americas Corporation
Product Type: Human OTC Drug
Drug Name: Shiseido Ultimate Sun Protection
Dosage Form: Topical Cream
Application #: part352
Rev. Date: 


NDC Package Codes:

  • 58411-359-10: 1 BOTTLE, PLASTIC IN 1 CARTON (58411‑359‑10) > 50 ML IN 1 BOTTLE, PLASTIC
  • 58411-359-11: 1 BOTTLE, PLASTIC IN 1 CARTON (58411‑359‑11) > 100 ML IN 1 BOTTLE, PLASTIC

Active Ingredients:

  • Avobenzone
  • Octinoxate
  • Octocrylene
  • Oxybenzone

Dosage Strength:

  • 1288 mg/50mL
  • 2524 mg/50mL
  • 2575 mg/50mL
  • 1545 mg/50mL

Related Products:

Based on records with the same trade name.
  • 58411-142 Shiseido Ultimate Sun Protection Topical Spray by Shiseido Americas Corporation
  • 58411-253 Shiseido Ultimate Sun Protection Topical Lotion by Shiseido Americas Corporation
  • 58411-254 Shiseido Ultimate Sun Protection Topical Cream by Shiseido Americas Corporation

NDC QR Code

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NDC 58411-359 QR Code

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.