63621-353 : Sundrops 67 .75 g/100ml Cutaneous Liquid


NDC: 63621-353
Labeler: Sunburst Chemicals, Inc.
Product Type: Human OTC Drug
Drug Name: Sundrops 67
Dosage Form: Cutaneous Liquid
Rev. Date: 


NDC Package Codes:

  • 63621-353-65: 1000 ML IN 1 BAG (63621‑353‑65)
  • 63621-353-80: 500 ML IN 1 BOTTLE, PUMP (63621‑353‑80)

Active Ingredients:

  • Chloroxylenol

Dosage Strength:

  • 7.5 mg/mL

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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.