10742-8149 : Rohto Relief Ophthalmic Liquid


NDC: 10742-8149
Labeler: The Mentholatum Company
Product Type: Human OTC Drug
Drug Name: Rohto Relief
Dosage Form: Ophthalmic Liquid
Application #: part349
Rev. Date: 


NDC Package Codes:

  • 10742-8149-1: 1 BOTTLE IN 1 CARTON (10742‑8149‑1) > 13 ML IN 1 BOTTLE

Active Ingredients:

  • Hypromelloses
  • Tetrahydrozoline Hydrochloride
  • Zinc Sulfate

Dosage Strength:

  • 2 mg/mL
  • .5 mg/mL
  • 2.5 mg/mL

Related Products:

Based on records with the same trade name.
  • 66613-8149 Rohto Relief Ophthalmic Liquid by Rohto Pharmaceutical Co Ltd
  • 75977-8149 Rohto Relief Ophthalmic Liquid by Rohto-mentholatum (Vietnam) Co. Ltd.

NDC QR Code

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NDC 10742-8149 QR Code

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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.