Home NDC 83804-016-01 Oimmal Gentle Eye Wash
Product NDC 83804-016
Requested package NDC 83804-016-01
11-digit product format 838040016
Labeler code 83804
Product ID 83804-016_4bb4e59b-a43f-fa38-e063-6294a90aea71
Type HUMAN OTC DRUG
Nonproprietary name SODIUM CHLORIDE
Dosage form LIQUID
Route INTRAOCULAR
Labeler Shenzhen Shandian Jingling Technology Co., Ltd.
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-02-26
Substance SODIUM CHLORIDE
Active strength .159 g/mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes openFDA label cross-check# Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Additional Listing Data#
Finished product Yes
Brand name base Oimmal Gentle Eye Wash
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM CHLORIDE .159 g/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 451W47IQ8X Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 83804-016-01 Oimmal Gentle Eye Wash 100 mL in 1 BOTTLE LIQUID 100 1
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 83804-016-01 83804001601 100 mL in 1 BOTTLE (83804-016-01) 100 ml 2026-02-26 No No Current