70738-001 : Lagom Cellus Sun Gel Topical Gel


NDC: 70738-001
Labeler: Skinmed International Co., Ltd.
Product Type: Human OTC Drug
Drug Name: Lagom Cellus Sun Gel
Dosage Form: Topical Gel
Application #: part352
Rev. Date: 


NDC Package Codes:

  • 70738-001-02: 1 CONTAINER IN 1 PACKAGE (70738‑001‑02) > 50 ML IN 1 CONTAINER (70738‑001‑01)

Active Ingredients:

  • Octinoxate
  • Octocrylene
  • Octisalate

Dosage Strength:

  • 3.5 mg/50mL
  • 2.5 mg/50mL
  • 2 mg/50mL

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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.