85053-002 : Woodsleep Tallow Sunscreen .0114 mg/57mg Topical Cream


NDC: 85053-002
Labeler: Shantou Woodsleep Biotechnology Co., Ltd.
Product Type: Human OTC Drug
Drug Name: Woodsleep Tallow Sunscreen
Dosage Form: Topical Cream
Application #: M020
Rev. Date: 


NDC Package Codes:

  • 85053-002-01: 57 MG IN 1 BOX (85053‑002‑01)

Active Ingredients:

  • Tallow

Dosage Strength:

  • .0114 mg/57mg

Related Products:

Based on records with the same trade name.
  • 85053-003 Woodsleep Tallow Sunscreen .012 mg/60mg Topical Cream by Shantou Woodsleep Biotechnology Co., Ltd.

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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.