RegenerEyes
- Manufacturer
- Regenerative Processing Plant, LLC
- Effective date
- 2021-11-19
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 22:04:44
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
(in each drop)
Glycerin, 0.4%
OTC - PURPOSE SECTION
Eye lubricant
INDICATIONS & USAGE SECTION
For the temporary relief of burning and irritation due to dryness of the eye.
For the temporary relief of discomfort due to minor irritation of the eye or to exposure to wind or sun
For use as a protectant against further irritation or to relieve dryness of the eye.
For use as a lubricant to prevent further irritation or to relieve dryness of the eye.
WARNINGS SECTION
Warnings
External Use Only
To avoid contamination, do not touch tip of the bottle closure to any surface(s) including the eye or the skin.
Stop use and ask a doctor if
You experience eye pain, changes in vision, continued redness, or irritation of the eye.
Condition worsens or persists for more than 72 hours.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children.
If swallowed, get medical help, or contact a Poison Control Center immediately.
DOSAGE & ADMINISTRATION SECTION
Instill 1 to 4 drops, one to four times per day in each eye, or as recommended by your eye care professional
INACTIVE INGREDIENT SECTION
d-MAPPS TM and 0.9% Sodium Chloride USP.
OTC - WHEN USING SECTION
Store at Room Temperature.
PATIENT COUNSELING INFORMATION
Questions? 1 800 781 0818
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Products#
Every source-derived product name is available through these pages.
- RegenerEyes LITE
- RegenerEyes
- GLYCERIN
- WATER
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 82305-002 | 82305-002-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| GLYCERIN | PDC6A3C0OX | ACTIB |
| WATER | 059QF0KO0R | 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 |
|---|---|---|---|---|---|---|
| e802dac6-b648-3287-e053-2a95a90aeefa | d1243811-c094-53f9-e053-2995a90abd74 | 2022-09-06 | Warnings | d1243811-c094-53f9-e053-2995a90abd74 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.

