Indications and uses
For the temporary relief of discomfort and redness of the eye due to minor eye irritations. For the temporary relief of burning & irritation due to dryness of the eye. For protection against further irritation.
Eyellic Eye Drops (Sterile)
- Manufacturer
- Hi-Healthcare Inc
- Effective date
- 2020-05-22
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 32618
- Source
- full-release
- Hydrated at
- 2026-05-31 23:14:17
Label at a glance#
ProductEyellic Eye Drops (Sterile)
Active ingredientHYPROMELLOSES, POLYSORBATE 80, NAPHAZOLINE HYDROCHLORIDE, ZINC SULFATE
Label structure13 sections
Dosage and administration
• Instill 1 or 2 drops in the affected eye(s) up to four times daily. • Children under 6 years of age, ask a doctor.
Contacts and useful links#
Websitewww.hi-healthcare.com
www.hi-healthcare.com
www.hi-healthcare.comLabel contents#
Full prescribing information#
Active Ingredients
Hypromelloses 0.2%
Polysorbate 80 0.5%
Naphazoline Hydrochloride 0.025%
Zinc Sulfate 0.25%
Purpose
Hypromelloses Lubricant
Polysorbate 80 Lubricant
Naphazoline Hydrochloride Redness Reliever
Zinc Sulfate Astringent
Uses
- For the temporary relief of discomfort and redness of the eye due to minor eye irritations.
- For the temporary relief of burning & irritation due to dryness of the eye.
- For protection against further irritation.
Directions
• Instill 1 or 2 drops in the affected eye(s) up to four times daily.
• Children under 6 years of age, ask a doctor.
Warnings
• For external use only.
• Do not use if solution changes color or becomes cloudy.
• Ask a doctor before use if you have narrow angle glaucoma.
When using this product
• Pupils may become enlarged temporarily.
• To avoid contamination, do not touch tip of container to any surface. Replace cap after using.
• Overuse may produce increased redness of the eye.
• Remove contact lens before using.
Stop use and ask a doctor if you experience
• eye pain.
• changes in vision.
• continued redness or irritation of the eye, or if the condition worsens or persists for more than 72 hours.
Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center right away.
Other information
• Some users may experience initial stinging sensation.
• Store at 15° to 25°C (59° to 77°F).
• Keep tightly closed.
• Use before expiration date marked on the carton and bottle.
Questions or Comments?
Contact Hi-Healthcare, Inc.
1-877-578-6288www.hi-healthcare.com
Distributed by Hi-Healthcare Inc.
Made in USA
Inactive ingredients
Boric Acid, Edetate Disodium, Polyaminopropyl Biguanide, Potassium Chloride, Water, Sodium Chloride, Sodium Citrate
Drug Facts Label
DailyMed Pharmacologic Classes#
| Class | Version | Type | Effective |
|---|---|---|---|
| ZINC CATION Pharmacologic Class Indexing | 2 | Indexing - Pharmacologic Class | 20180813 |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 77684-899-01 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-7361-a426-e053-dadaa90af4c2 | Hi-Healthcare Inc |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 77684-899-01 | Eyellic Eye Drops (Sterile) | 15 mL in 1 BOTTLE, DROPPER | SOLUTION/ DROPS | 15 | 32618 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Eyellic Eye Drops (Sterile)
- Eye Drops
- HYPROMELLOSES
- POLYSORBATE 80
- NAPHAZOLINE HYDROCHLORIDE
- NAPHAZOLINE
- ZINC SULFATE
- ZINC CATION
- BORIC ACID
- EDETATE DISODIUM
- POLYAMINOPROPYL BIGUANIDE HYDROCHLORIDE
- POTASSIUM CHLORIDE
- WATER
- SODIUM CHLORIDE
- SODIUM CITRATE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 77684-899 | 77684-899-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| HYPROMELLOSES | 3NXW29V3WO | ACTIB |
| POLYSORBATE 80 | 6OZP39ZG8H | ACTIB |
| NAPHAZOLINE HYDROCHLORIDE | MZ1131787D | ACTIB |
| ZINC SULFATE | 89DS0H96TB | ACTIB |
| BORIC ACID | R57ZHV85D4 | IACT |
| EDETATE DISODIUM | 7FLD91C86K | IACT |
| POLYAMINOPROPYL BIGUANIDE HYDROCHLORIDE | 6P1MZW6VKY | IACT |
| POTASSIUM CHLORIDE | 660YQ98I10 | IACT |
| WATER | 059QF0KO0R | IACT |
| SODIUM CHLORIDE | 451W47IQ8X | IACT |
| SODIUM CITRATE | 1Q73Q2JULR | IACT |
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| de7f68f6-a924-4b43-8aa0-559d4e988592 | 18961f24-d50a-4d62-9977-85381fb03eae | 2020-05-22 | Warnings | de7f68f6-a924-4b43-8aa0-559d4e988592 18961f24-d50a-4d62-9977-85381fb03eae |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.