71975-070 : Ultra V Idebenone Sunblock Topical Cream


NDC: 71975-070
Labeler: Ultra V Co., Ltd
Product Type: Human OTC Drug
Drug Name: Ultra V Idebenone Sunblock
Dosage Form: Topical Cream
Application #: part352
Rev. Date: 


NDC Package Codes:

  • 71975-070-02: 1 TUBE IN 1 CARTON (71975‑070‑02) > 50 ML IN 1 TUBE (71975‑070‑01)

Active Ingredients:

  • Homosalate
  • Avobenzone
  • Ensulizole

Dosage Strength:

  • 5 g/50mL
  • 1.75 g/50mL
  • 1.75 g/50mL

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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.