FDA.reportPublic FDA data

Droptics Performance Eye Drops

Manufacturer
Droptics LLC
Effective date
2026-02-09
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
full-release
Hydrated at
2026-06-01 01:37:35

Label at a glance#

ProductDroptics Performance Eye Drops
Active ingredientNAPHAZOLINE HYDROCHLORIDE, PROPYLENE GLYCOL
Label structure8 sections

Indications and uses

Temporarily relieves burning and irritation due to dryness of the eye Relieves redness of the eye due to minor eye irritations

Dosage and administration

Put 1 or 2 drops in the affected eye(s) up to 4 times daily Tightly screw on cap to seal after use

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Naphozoline Hydrochloride 0.03%
Propylene Glycol: 1.0%

Purpose

OTC - PURPOSE SECTION

Redness Reliver
Lubricant

Uses

INDICATIONS & USAGE SECTION

Temporarily relieves burning and irritation due to dryness of the eye
Relieves redness of the eye due to minor eye irritations

Warnings

WARNINGS SECTION

For external use only
Ask a doctor before use if you have narrow angle glaucoma
When using this product
• Do not touch tip of container to any surface to avoid contamination
• Replace each cap after each use
• Do not use if solution changes color or becomes cloudy
• Overuse may cause more eye redness
• Pupils may become enlarged temporarily
• Remove contact lenses before use
Stop Use and ask a doctor if
• You feel eye pain
• Changes in vision occur
• Redness or irritation of the eyes lasts
• Condition worsens or lasts more than 72 hours
Keep out of reach of children
• If swallowed, get medical help or contact a Poison Control center right away

Directions

DOSAGE & ADMINISTRATION SECTION

Put 1 or 2 drops in the affected eye(s) up to 4 times daily

  • Tightly screw on cap to seal after use

Other information

SPL UNCLASSIFIED SECTION

Store at 20 - 25°C (68 -77°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

benzalkonium chloride, boric acid, borneol, caffeine, camphor, menthol, potassium l-aspartate, purified water, taurine

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage descriptionimage descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2627786naphazoline hydrochloride 0.03 % / propylene glycol 1 % Ophthalmic SolutionPSN7
2627786naphazoline hydrochloride 0.3 MG/ML / propylene glycol 10 MG/ML Ophthalmic SolutionSCD7
2627786naphazoline hydrochloride 0.03 % / propylene glycol 1 % Ophthalmic SolutionSY7

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7dea7767-9f52-b60a-5435-33cb9cc28baeProduct name420250124
6338270f-96cb-0ecb-6fbb-0a9bc78001f4Product name720250116
0ca83774-3f79-b837-5d6f-c210102f3bc8Product name620250114
41b814f3-0166-1c53-c9ef-a0794c7daf9dProduct name320221110
a590be26-846c-8659-a5a1-fb25907965dcProduct name220221110
2dc76302-91c0-4c35-ad78-99adfb049c4bProduct name120200603
e6065d4b-5ae1-476f-a40e-f2851cbb5d2bProduct name220180221
f212291f-05fe-9603-fc7e-bd73e38ce1e6Product name220161129
182f9ab4-4ab5-c449-200f-87ce2ce8e550Product name220151105
332e86c3-7875-ca6e-f934-2206d2b31996Product name120140508
56625fcc-aa34-9d30-d0e9-1c1beb37ea21Product name120140508
7dfac40f-a405-cd2e-7c06-3059ec0e1092Product name120140508
96c2be53-8e44-452d-56a2-d255b2f1af2dProduct name120140508
bf8bd5f7-495f-4022-2780-7ded7ea7ea44Product name120140508
d223c173-c39b-d764-47d4-d671d3088815Product name120140508
e01133ad-4dcd-c7f3-454b-2ff569ee160aProduct name120140508
e18001c8-33ae-5f66-9cdc-a39724bd4573Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85211-001-01Droptics Performance Eye Drops1 in 1 CARTONLIQUID17
85211-001-01Droptics Performance Eye Drops5 mL in 1 BOTTLE, DROPPERLIQUID57
85211-001-02Droptics Performance Eye Drops7 mL in 1 BOTTLE, DROPPERLIQUID77
85211-001-02Droptics Performance Eye Drops1 in 1 CARTONLIQUID17

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85211-00185211-001-01, 85211-001-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7IACT
BORIC ACIDR57ZHV85D4IACT
BORNEOLM89NIB437XIACT
CAFFEINE3G6A5W338EIACT
CAMPHOR (SYNTHETIC)5TJD82A1ETIACT
MENTHOLL7T10EIP3AIACT
POTASSIUM ASPARTATEOC4598NZEQIACT
WATER059QF0KO0RIACT
TAURINE1EQV5MLY3DIACT
NAPHAZOLINE HYDROCHLORIDEMZ1131787DACTIB
PROPYLENE GLYCOL6DC9Q167V3ACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
52025-12-05monthly-update2026-06-03 17:45:27

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Droptics Performance Eye DropsNAPHAZOLINE HYDROCHLORIDE, PROPYLENE GLYCOLDroptics LLC20fd6822-a7fd-4593-92bb-0a07260893e22026-02-09WarningsExact identifier
ndc (package): 85211-001-02
ndc (package): 85211-001-01
ndc (product): 85211-001
ndc11 (package): 85211000102
ndc11 (package): 85211000101
spl id: 4a69ff43-04d2-a9c5-e063-6294a90a84a8
spl set id: 20fd6822-a7fd-4593-92bb-0a07260893e2

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.