87170-001 : Hampton Sun Topical Gel


NDC: 87170-001
Labeler: Hampton Sun
Product Type: Human OTC Drug
Drug Name: Hampton Sun
Dosage Form: Topical Gel
Application #: M020
Rev. Date: 


NDC Package Codes:

  • 87170-001-01: 118 G IN 1 BOTTLE, PLASTIC (87170‑001‑01)

Active Ingredients:

  • Octinoxate
  • Oxybenzone

Dosage Strength:

  • 4 g/100g
  • 2 g/100g

Related Products:

Based on records with the same trade name.
  • 87170-002 Hampton Sun Topical Spray by Hampton Sun
  • 72667-011 Hampton Sun Topical Spray by Inspec Solutions LLC.
  • 72667-012 Hampton Sun Topical Gel by Inspec Solutions LLC.

NDC 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.