72839-389 : Spf 50 Sunscreen Topical Spray


NDC: 72839-389
Labeler: Derma Care Research Labs, LLC
Product Type: Human OTC Drug
Drug Name: Spf 50 Sunscreen
Dosage Form: Topical Spray
Application #: M020
Rev. Date: 


NDC Package Codes:

  • 72839-389-06: 170 G IN 1 CAN (72839‑389‑06)
  • 72839-389-16: 170 G IN 1 CAN (72839‑389‑16)
  • 72839-389-26: 170 G IN 1 CAN (72839‑389‑26)
  • 72839-389-36: 170 G IN 1 CAN (72839‑389‑36)

Active Ingredients:

  • Avobenzone
  • Homosalate
  • Octisalate
  • Octocrylene

Dosage Strength:

  • 3 g/100g
  • 15 g/100g
  • 5 g/100g
  • 10 g/100g

Related Products:

Based on records with the same trade name.
  • 11344-059 Spf 50 Sunscreen Topical Lotion by Consumer Product Partners, LLC
  • 53942-001 Spf 50 Sunscreen Topical Aerosol, Spray by Demoulas Super Markets, Inc
  • 53942-003 Spf 50 Sunscreen Topical Lotion by Demoulas Super Markets, Inc
  • 71585-115 Spf 50 Sunscreen 225 mg/g Topical Stick by Salt and Stone LLC

NDC QR Code

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NDC 72839-389 QR Code

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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.