52686-228 : Shiseido White Lucent Topical Emulsion


NDC: 52686-228
Labeler: Shiseido America Inc.
Product Type: Human OTC Drug
Drug Name: Shiseido White Lucent
Dosage Form: Topical Emulsion
Application #: part352
Rev. Date: 


NDC Package Codes:

  • 52686-228-10: 1 BOTTLE, PUMP IN 1 CARTON (52686‑228‑10) > 71 G IN 1 BOTTLE, PUMP

Active Ingredients:

  • Octinoxate
  • Octocrylene

Dosage Strength:

  • 3.479 g/71g
  • 3.55 g/71g

Related Products:

Based on records with the same trade name.
  • 52686-227 Shiseido White Lucent Topical Cream by Shiseido America Inc.

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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.