0869-0109 : Sunscreen Topical Spray


NDC0869-0109
Labeler: Vi-jon, LLC
Product Type: Human OTC Drug
Drug Name: Sunscreen
Dosage Form: Topical Spray
Application #: part352
Rev. Date: 


NDC Package Codes:

  • 0869-0109-14: 177.6 ML IN 1 CAN (0869‑0109‑14)

Active Ingredients:

  • Avobenzone
  • Homosalate
  • Octisalate
  • Octocrylene

Dosage Strength:

  • 30 mg/mL
  • 100 mg/mL
  • 50 mg/mL
  • 70 mg/mL

Related Products:

Based on records with the same trade name.

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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.