Home NDC 81488-001-15 Mineffect eye drops
Product NDC 81488-001
Requested package NDC 81488-001-15
11-digit product format 814880001
Labeler code 81488
Product ID 81488-001_17047ea2-bae2-044a-e063-6294a90a4932
Type HUMAN OTC DRUG
Nonproprietary name Alumina Silicata, Calcarea Fluorica, Ferrum Metallicum, Ferrum Phosphoricum, Natrum Muriaticum, Phosphorus, Sulphur, Titanium Metallicum, Zincum Metallicum
Dosage form SOLUTION/ DROPS
Route OPHTHALMIC
Labeler Kadesh Incoporation Co,Ltd
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2021-02-01
Substance CALCIUM FLUORIDE; FERROSOFERRIC PHOSPHATE; IRON; KAOLIN; PHOSPHORUS; SODIUM CHLORIDE; SULFUR; TITANIUM; ZINC
Active strength 6; 7; 7; 5; 6; 4; 4; 7; 8 [hp_X]/15mL; [hp_X]/15mL; [hp_X]/15mL; [hp_X]/15mL; [hp_X]/15mL; [hp_X]/15mL; [hp_X]/15mL; [hp_X]/15mL; [hp_X]/15mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 1 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2024-03-11 06:39 UTC · source 2024-03-08 excluded package package 81488-001 81488-001-15 I Inactivated by FDA excluded / ndc_excluded.zip 1332a3947898…d4bfe170f9cd…
Additional Listing Data#
Finished product Yes
Brand name base Mineffect eye drops
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength KAOLIN 6 [hp_X]/15mL CALCIUM FLUORIDE 7 [hp_X]/15mL IRON 7 [hp_X]/15mL FERROSOFERRIC PHOSPHATE 5 [hp_X]/15mL SODIUM CHLORIDE 6 [hp_X]/15mL PHOSPHORUS 4 [hp_X]/15mL SULFUR 4 [hp_X]/15mL TITANIUM 7 [hp_X]/15mL ZINC 8 [hp_X]/15mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 9 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 81488-001-15 Mineffect eye drops 15 mL in 1 BOTTLE, DROPPER SOLUTION/ DROPS 15 2 81488-001-15 Mineffect eye drops 1 in 1 BOX SOLUTION/ DROPS 1 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 81488-001 MINEFFECT EYE DROPS (ALUMINA SILICATA, CALCAREA FLUORICA, FERRUM METALLICUM, FERRUM PHOSPHORICUM, NATRUM MURIATICUM, PHOSPHORUS, SULPHUR, TITANIUM METALLICUM, ZINCUM METALLICUM) SOLUTION/ DROPS [KADESH INCOPORATION CO,LTD] 2 Current NDC, Legacy NDC, 2 package rows 20240427_e2259f58-3043-4af3-918d-d4403757aa1f.zip
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 1 of 1 · 1 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Mineffect eye drops ALUMINA SILICATA, CALCAREA FLUORICA, FERRUM METALLICUM, FERRUM PHOSPHORICUM, NATRUM MURIATICUM, PHOSPHORUS, SULPHUR, TITANIUM METALLICUM, ZINCUM METALLICUM Kadesh Incoporation Co,Ltd e2259f58-3043-4af3-918d-d4403757aa1f 2024-04-26 Warnings Exact identifier ndc (package): 81488-001-15 ndc (product): 81488-001 ndc11 (package): 81488000115
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 81488-001-15 81488000115 1 BOTTLE, DROPPER in 1 BOX (81488-001-15) / 15 mL in 1 BOTTLE, DROPPER 2021-02-01 0000-00-00 No No Current