NDC 10742-8143

Rohto Ice

Hypromellose, Tetrahydrozoline Hydrochloride, Zinc Sulfate

Rohto Ice is a Ophthalmic Liquid in the Human Otc Drug category. It is labeled and distributed by The Mentholatum Company. The primary component is Hypromellose, Unspecified; Tetrahydrozoline Hydrochloride; Zinc Sulfate, Unspecified Form.

• Product ID: 10742-8143_011c1316-c1d5-453f-8c5c-4c08eb31b3f6
• NDC: 10742-8143
• Product Type: Human Otc Drug
• Proprietary Name: Rohto Ice
• Generic Name: Hypromellose, Tetrahydrozoline Hydrochloride, Zinc Sulfate
• Dosage Form: Liquid
• Route of Administration: OPHTHALMIC
• Marketing Start Date: 2005-09-27
• Marketing Category: OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
• Application Number: part349
• Labeler Name: The Mentholatum Company
• Substance Name: HYPROMELLOSE, UNSPECIFIED; TETRAHYDROZOLINE HYDROCHLORIDE; ZINC SULFATE, UNSPECIFIED FORM
• Active Ingredient Strength: 2 mg/mL; mg/mL; mg/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 10742-8143-1

1 BOTTLE, WITH APPLICATOR in 1 CARTON (10742-8143-1) > 13 mL in 1 BOTTLE, WITH APPLICATOR

• Marketing Start Date: 2005-09-27
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 10742-8143-1 [10742814301]

Rohto Ice LIQUID

• Marketing Category: OTC monograph final
• Application Number: part349
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2005-09-27

Drug Details

Active Ingredients

Ingredient	Strength
HYPROMELLOSE, UNSPECIFIED	2 mg/mL

OpenFDA Data

• SPL SET ID: 209bcec8-fbb4-4079-8ae2-810c48f3de93
• Manufacturer:
  • The Mentholatum Company
• UNII:
  • 89DS0H96TB
  • 0YZT43HS7D
  • 3NXW29V3WO
• RxNorm Concept Unique ID - RxCUI:
  • 1098640

NDC Crossover Matching brand name "Rohto Ice" or generic name "Hypromellose, Tetrahydrozoline Hydrochloride, Zinc Sulfate"

NDC	Brand Name	Generic Name
10742-8143	Rohto	Hypromellose, Tetrahydrozoline hydrochloride, Zinc sulfate
10742-8146	Rohto	Hypromellose, Tetrahydrozoline hydrochloride, Zinc sulfate