Indications and uses
For use as a lubricant to prevent further irritaion or to relieve dryness of the eye
Hypromellose Eye Drops 0.7%
- Manufacturer
- Aurolab
- Effective date
- 2025-01-02
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 6
- Source
- full-release
- Hydrated at
- 2026-06-01 00:50:35
Label at a glance#
ProductHypromellose Eye Drops 0.7%
Active ingredientHYPROMELLOSE 2910 (4000 MPA.S)
Label structure14 sections
Dosage and administration
lnstill 1or 2 drops in the affected eye, as needed
Contacts and useful links#
Websitewww.aurolab.com
www.aurolab.com
www.aurolab.comLabel contents#
Full prescribing information#
Active Ingredient
Hypromellose 0.7% BP w/v
DIRECTIONS FOR USE
- lnstill 1or 2 drops in the affected eye, as needed
INACTIVE INGREDIENT
- Benzalkonium Chloride
- Borax
- Boric acid
- EDTA disodium salt
- Potassium chloride
- Purified water
- Sodiumchloride
Tamper Protection
- For your protection a tamper evident ring is attached to the bottlecap
- Upon opening, this will separate from the cap and can be discarded
- Use only if this ring is present and attached when the bottle is first opened
USE
- For use as a lubricant to prevent further irritation or to relieve dryness of the eye
Questions
KEEP OUT OF REACH OF CHILDREN
- If swallowed, get medical help or contact a poison control center right away
ASK DOCTOR
- If you experience eye pain
- Change in vision
- Continued redness(or) irritation of the eye
- Condition worsens or persists for more than 72 hours
DO NOT USE
- If you are sensitive to any ingredient in this product
- If solution changes color or becomes cloudy
Dosage
Instill 1 or 2 drops in the affected eyes as needed
Warnings
For External Use Only
Indications and Usage
For use as a lubricant to prevent further irritaion or to relieve dryness of the eye
Eye Lubricant
Eye Lubricant
CARTON LABEL
DailyMed Product Concepts#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 16030-101-10 | Hypromellose Eye Drops 0.7% | 10 mL in 1 BOTTLE, DROPPER | FOR SOLUTION | 10 | 6 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Hypromellose Eye Drops 0.7%
- BORIC ACID
- WATER
- HYPROMELLOSE 2910 (4000 MPA.S)
- BENZALKONIUM CHLORIDE
- SODIUM BORATE
- POTASSIUM CHLORIDE
- SODIUM CHLORIDE
- EDETATE DISODIUM
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 16030-101 | 16030-101-10 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| BORIC ACID | R57ZHV85D4 | IACT |
| WATER | 059QF0KO0R | IACT |
| HYPROMELLOSE 2910 (4000 MPA.S) | RN3152OP35 | ACTIB |
| BENZALKONIUM CHLORIDE | F5UM2KM3W7 | IACT |
| SODIUM BORATE | 91MBZ8H3QO | IACT |
| POTASSIUM CHLORIDE | 660YQ98I10 | IACT |
| SODIUM CHLORIDE | 451W47IQ8X | IACT |
| EDETATE DISODIUM | 7FLD91C86K | 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 |
|---|---|---|---|---|---|---|
| Hypromellose Eye Drops 0.7% | HYPROMELLOSE EYE DROPS 0.7% | Aurolab | d35313d0-b190-5fb0-e053-2a95a90a5283 | 2025-01-02 | Warnings | 16030-101-10 16030-101 16030010110 2ac6c72f-6f81-825c-e063-6294a90af661 d35313d0-b190-5fb0-e053-2a95a90a5283 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.