66613-8144 : Rohto Arctic Ophthalmic Liquid


NDC: 66613-8144
Labeler: Rohto Pharmaceutical Co Ltd
Product Type: Human OTC Drug
Drug Name: Rohto Arctic
Dosage Form: Ophthalmic Liquid
Application #: part349
Rev. Date: 


NDC Package Codes:

  • 66613-8144-1: 1 BOTTLE IN 1 CARTON (66613‑8144‑1) > 13 ML IN 1 BOTTLE

Active Ingredients:

  • Hypromelloses
  • Tetrahydrozoline Hydrochloride

Dosage Strength:

  • 3.5 mg/mL
  • .5 mg/mL

Related Products:

Based on records with the same trade name.
  • 10742-8144 Rohto Ophthalmic Liquid by The Mentholatum Company
  • 75977-8144 Rohto Arctic Ophthalmic Liquid by Rohto-mentholatum (Vietnam) 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.