rohto ice

Generic: hypromellose, tetrahydrozoline hydrochloride, zinc sulfate

Labeler: the mentholatum company
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name rohto ice
Generic Name hypromellose, tetrahydrozoline hydrochloride, zinc sulfate
Labeler the mentholatum company
Dosage Form LIQUID
Routes
OPHTHALMIC
Active Ingredients

hypromellose, unspecified 2 mg/mL, tetrahydrozoline hydrochloride .5 mg/mL, zinc sulfate, unspecified form 2.5 mg/mL

Manufacturer
The Mentholatum Company

Identifiers & Regulatory

Product NDC 10742-8143
Product ID 10742-8143_2978c996-d366-daff-e063-6394a90abe0b
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M018
Listing Expiration 2026-12-31
Marketing Start 2005-09-27

Pharmacologic Class

Classes
copper absorption inhibitor [epc] decreased copper ion absorption [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 107428143
Hyphenated Format 10742-8143

Supplemental Identifiers

RxCUI
1098640
UPC
0310742010862
UNII
3NXW29V3WO 0YZT43HS7D 89DS0H96TB

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name rohto ice (source: ndc)
Generic Name hypromellose, tetrahydrozoline hydrochloride, zinc sulfate (source: ndc)
Application Number M018 (source: ndc)
Routes
OPHTHALMIC
source: ndc

Resolved Composition

Strengths
  • 2 mg/mL
  • .5 mg/mL
  • 2.5 mg/mL
source: ndc
Packaging
  • 1 BOTTLE, WITH APPLICATOR in 1 CARTON (10742-8143-1) / 13 mL in 1 BOTTLE, WITH APPLICATOR
source: ndc

Packages (1)

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

Ingredients (3)

hypromellose, unspecified (2 mg/mL) tetrahydrozoline hydrochloride (.5 mg/mL) zinc sulfate, unspecified form (2.5 mg/mL)

Linked Drug Pages (1)

Rohto Ice ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["OPHTHALMIC"], "spl_id": "2978c996-d366-daff-e063-6394a90abe0b", "openfda": {"upc": ["0310742010862"], "unii": ["3NXW29V3WO", "0YZT43HS7D", "89DS0H96TB"], "rxcui": ["1098640"], "spl_set_id": ["209bcec8-fbb4-4079-8ae2-810c48f3de93"], "manufacturer_name": ["The Mentholatum Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, WITH APPLICATOR in 1 CARTON (10742-8143-1)  / 13 mL in 1 BOTTLE, WITH APPLICATOR", "package_ndc": "10742-8143-1", "marketing_start_date": "20050927"}], "brand_name": "Rohto Ice", "product_id": "10742-8143_2978c996-d366-daff-e063-6394a90abe0b", "dosage_form": "LIQUID", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "10742-8143", "generic_name": "Hypromellose, Tetrahydrozoline hydrochloride, Zinc sulfate", "labeler_name": "The Mentholatum Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Rohto", "brand_name_suffix": "Ice", "active_ingredients": [{"name": "HYPROMELLOSE, UNSPECIFIED", "strength": "2 mg/mL"}, {"name": "TETRAHYDROZOLINE HYDROCHLORIDE", "strength": ".5 mg/mL"}, {"name": "ZINC SULFATE, UNSPECIFIED FORM", "strength": "2.5 mg/mL"}], "application_number": "M018", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20050927", "listing_expiration_date": "20261231"}