Home NDC 87354-002 Regener-Eyes Ophthalmic Solution PROFESSIONAL STRENGTH XL
Product NDC 87354-002
11-digit product format 873540002
Labeler code 87354
Product ID 87354-002_498954b3-bc1e-0b1b-e063-6294a90ab074
Type HUMAN OTC DRUG
Nonproprietary name Glycerin Ophthalmic Solution
Dosage form SOLUTION/ DROPS
Route OPHTHALMIC
Labeler M & M PRODUCTS, L.L.C.
Application M018
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-02-01
Substance GLYCERIN
Active strength 5 mg/mL
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Glycerol [CS], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Chemical Allergen [EPC]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Regener-Eyes Ophthalmic Solution PROFESSIONAL STRENGTH XL
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength GLYCERIN 5 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination PDC6A3C0OX Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2540675 Internal RxNorm lookup 2609932 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 87354-002-01 Regener-Eyes Ophthalmic Solution PROFESSIONAL STRENGTH XL 1 mL in 1 BOTTLE SOLUTION/ DROPS 1 2 87354-002-01 Regener-Eyes Ophthalmic Solution PROFESSIONAL STRENGTH XL 1 in 1 CARTON SOLUTION/ DROPS 1 2
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 6 of 25 · 494 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 87354-002-01 87354000201 1 BOTTLE in 1 CARTON (87354-002-01) / 1 mL in 1 BOTTLE 1 bottle 2026-02-01 No No Current