Indications and uses
for the temporary relief of burning & irritation due to dryness of the eye for use as a protectant against further irritation or to relieve dryness of the eye relieves redness of the eye due to minor eye irritations
Multi- Action Relief Drops
- Manufacturer
- RITE AID
- Effective date
- 2022-04-06
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 22:04:15
Label at a glance#
ProductMulti- Action Relief Drops
Active ingredientPOLYVINYL ALCOHOL, UNSPECIFIED, POVIDONE, TETRAHYDROZOLINE HYDROCHLORIDE
Label structure12 sections
Dosage and administration
Instill 1 to 2 drops in the affected eye(s) up to four times daily.
Contacts and useful links#
Label contents#
Full prescribing information#
SPL UNCLASSIFIED SECTION
Drug Facts
Active ingredients
Polyvinyl alcohol 0.5%
Active ingredients
Povidone 0.6%
Purpose
Lubricant
Active ingredient
Tetrahydrozoline hydrochloride 0.05%
Purpose
Redness reliever
Uses
- for the temporary relief of burning & irritation due to dryness of the eye
- for use as a protectant against further irritation or to relieve dryness of the eye
- relieves redness of the eye due to minor eye irritations
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
- to avoid contamination, do not touch tip to any surface
- replace cap after using
- overuse may produce increased redness of the eye
- pupils may become enlarged temporarily
Stop use & ask a doctor if
- you experience eye pain
- you experience changes in vision
- you experience continued redness or irritation of the eye
- the condition worsens
- symptoms last for more than 72 hours
Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center(1-800-222-1222) right away.
Directions
Instill 1 to 2 drops in the affected eye(s) up to four times daily.
Other information
- store at room temperature
- remove contact lenses before using
- retain carton for future reference
Inactive ingredients
benzalkonium chloride, disodium hydrogen phosphate, edetate disodium, mannitol, sodium dihydrogen phosphate dihydrate, potassium chloride, purified water, sodium chloride, sodium citrate.
May contain hydrochloric acid and/or sodium hydroxide to adjust pH.
PRINCIPAL DISPLAY PANEL
Products#
Every source-derived product name is available through these pages.
- Multi- Action Relief Drops
- Polyvinyl Alcohol and Povidone and Tetrahydrozoline Hydrochloride
- BENZALKONIUM CHLORIDE
- SODIUM PHOSPHATE, MONOBASIC, DIHYDRATE
- SODIUM PHOSPHATE, DIBASIC, ANHYDROUS
- EDETATE DISODIUM
- MANNITOL
- POTASSIUM CHLORIDE
- WATER
- SODIUM CHLORIDE
- SODIUM CITRATE
- POLYVINYL ALCOHOL, UNSPECIFIED
- POVIDONE
- TETRAHYDROZOLINE HYDROCHLORIDE
- TETRAHYDROZOLINE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 11822-2254 | 11822-2254-3 |
Ingredients#
Every source-derived ingredient row is available through these pages.
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 |
|---|---|---|---|---|---|---|
| 0fa88807-8112-7b5e-e063-6294a90aef67 | dc021bba-8f1f-c342-e053-2995a90a185c | 2024-01-23 | Warnings | dc021bba-8f1f-c342-e053-2995a90a185c |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.