58443-0126 : Ulta Topical Lotion


NDC: 58443-0126
Labeler: Prime Enterprises, Inc.
Product Type: Human OTC Drug
Drug Name: Ulta Sunscreen Spf 15
Dosage Form: Topical Lotion
Application #: part352
Rev. Date: 


NDC Package Codes:

  • 58443-0126-4: 177 ML IN 1 TUBE (58443‑0126‑4)

Active Ingredients:

  • Octisalate
  • Oxybenzone
  • Octinoxate

Dosage Strength:

  • 27.9 mg/mL
  • 18.6 mg/mL
  • 46.5 mg/mL

Related Products:

Based on records with the same trade name.
  • 62296-8210 Ulta Sunscreen Spf 15 Topical Lotion by Ulta

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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.