clear eyes maximum itchy eye relief

Generic: glycerin and naphazoline hydrochloride and zinc sulfate

Labeler: prestige brands holdings, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name clear eyes maximum itchy eye relief
Generic Name glycerin and naphazoline hydrochloride and zinc sulfate
Labeler prestige brands holdings, inc.
Dosage Form LIQUID
Routes
OPHTHALMIC
Active Ingredients

glycerin 2.5 mg/mL, naphazoline hydrochloride .12 mg/mL, zinc sulfate 2.5 mg/mL

Manufacturer
Prestige Brands Holdings, Inc.

Identifiers & Regulatory

Product NDC 67172-999
Product ID 67172-999_4ed44e8e-1743-4724-83ce-d6d1c69677f5
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M018
Listing Expiration 2026-12-31
Marketing Start 2011-03-15

Pharmacologic Class

Established (EPC)
non-standardized chemical allergen [epc]
Chemical Structure
allergens [cs] glycerol [cs]
Physiologic Effect
increased histamine release [pe] cell-mediated immunity [pe] increased igg production [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 67172999
Hyphenated Format 67172-999

Supplemental Identifiers

RxCUI
1046644
UNII
PDC6A3C0OX MZ1131787D 89DS0H96TB
NUI
N0000185370 N0000175629 N0000184306 N0000185001 M0000728 M0009417

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 clear eyes maximum itchy eye relief (source: ndc)
Generic Name glycerin and naphazoline hydrochloride and zinc sulfate (source: ndc)
Application Number M018 (source: ndc)
Routes
OPHTHALMIC
source: ndc

Resolved Composition

Strengths
  • 2.5 mg/mL
  • .12 mg/mL
source: ndc
Packaging
  • 1 BOTTLE, DROPPER in 1 BOX (67172-999-01) / 15 mL in 1 BOTTLE, DROPPER
  • 1 BOTTLE, DROPPER in 1 CARTON (67172-999-06) / 6 mL in 1 BOTTLE, DROPPER
source: ndc

Packages (2)

Ingredients (3)

glycerin (2.5 mg/mL) naphazoline hydrochloride (.12 mg/mL) zinc sulfate (2.5 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "4ed44e8e-1743-4724-83ce-d6d1c69677f5", "openfda": {"nui": ["N0000185370", "N0000175629", "N0000184306", "N0000185001", "M0000728", "M0009417"], "unii": ["PDC6A3C0OX", "MZ1131787D", "89DS0H96TB"], "rxcui": ["1046644"], "spl_set_id": ["326a1462-78d1-42d6-8257-7e4f00d1f215"], "pharm_class_cs": ["Allergens [CS]", "Glycerol [CS]"], "pharm_class_pe": ["Increased Histamine Release [PE]", "Cell-mediated Immunity [PE]", "Increased IgG Production [PE]"], "pharm_class_epc": ["Non-Standardized Chemical Allergen [EPC]"], "manufacturer_name": ["Prestige Brands Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, DROPPER in 1 BOX (67172-999-01)  / 15 mL in 1 BOTTLE, DROPPER", "package_ndc": "67172-999-01", "marketing_start_date": "20110315"}, {"sample": false, "description": "1 BOTTLE, DROPPER in 1 CARTON (67172-999-06)  / 6 mL in 1 BOTTLE, DROPPER", "package_ndc": "67172-999-06", "marketing_start_date": "20180904"}], "brand_name": "Clear Eyes Maximum Itchy Eye Relief", "product_id": "67172-999_4ed44e8e-1743-4724-83ce-d6d1c69677f5", "dosage_form": "LIQUID", "pharm_class": ["Allergens [CS]", "Cell-mediated Immunity [PE]", "Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]", "Glycerol [CS]", "Increased Histamine Release [PE]", "Increased IgG Production [PE]", "Non-Standardized Chemical Allergen [EPC]"], "product_ndc": "67172-999", "generic_name": "Glycerin and Naphazoline Hydrochloride and Zinc Sulfate", "labeler_name": "Prestige Brands Holdings, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Clear Eyes Maximum Itchy Eye Relief", "active_ingredients": [{"name": "GLYCERIN", "strength": "2.5 mg/mL"}, {"name": "NAPHAZOLINE HYDROCHLORIDE", "strength": ".12 mg/mL"}, {"name": "ZINC SULFATE", "strength": "2.5 mg/mL"}], "application_number": "M018", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20110315", "listing_expiration_date": "20261231"}