10742-8175 : Rohto Digi-eye Ophthalmic Liquid


NDC: 10742-8175
Labeler: The Mentholatum Company
Product Type: Human OTC Drug
Drug Name: Rohto Digi-eye
Dosage Form: Ophthalmic Liquid
Application #: part349
Rev. Date: 


NDC Package Codes:

  • 10742-8175-1: 1 BOTTLE, WITH APPLICATOR IN 1 CARTON (10742‑8175‑1) > 13 ML IN 1 BOTTLE, WITH APPLICATOR

Active Ingredients:

  • Hypromellose
  • Unspecified
  • Tetrahydrozoline Hydrochloride

Dosage Strength:

  • 3.5 mg/mL
  • .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.