58232-0753 : Lubriderm Daily Moisture Topical Lotion


NDC: 58232-0753
Labeler: Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc.
Product Type: Human OTC Drug
Drug Name: Lubriderm Daily Moisture Sunscreen Broad Spectrum Spf15
Dosage Form: Topical Lotion
Application #: part352
Rev. Date: 


NDC Package Codes:

  • 58232-0753-1: 400 ML IN 1 BOTTLE, PUMP (58232‑0753‑1)

Active Ingredients:

  • Avobenzone
  • Octisalate
  • Octocrylene
  • Oxybenzone

Dosage Strength:

  • 20 mg/mL
  • 40 mg/mL
  • 30 mg/mL
  • 22 mg/mL

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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.