Home NDC 79481-0125-1 Meijer Antibacterial Spring Rain Hand
Product NDC 79481-0125
Requested package NDC 79481-0125-1
11-digit product format 794810125
Labeler code 79481
Product ID 79481-0125_570060e8-b3b5-e4c4-e063-6394a90a9bde
Type HUMAN OTC DRUG
Nonproprietary name Benzalkonium Chloride
Dosage form SOAP
Route TOPICAL
Labeler Meijer, Inc.
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-12-05
Substance BENZALKONIUM CHLORIDE
Active strength .13 g/100mL
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 Meijer Antibacterial Spring Rain Hand
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZALKONIUM CHLORIDE .13 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination F5UM2KM3W7 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1046593 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 79481-0125-1 Meijer Antibacterial Spring Rain Hand 1650 mL in 1 BOTTLE SOAP 1650 1 79481-0125-2 Meijer Antibacterial Spring Rain Hand 332 mL in 1 BOTTLE, PUMP SOAP 332 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 79481-0125 MEIJER ANTIBACTERIAL SPRING RAIN HAND (BENZALKONIUM CHLORIDE) SOAP MEIJER ANTIBACTERIAL AMBER HAND (BENZALKONIUM CHLORIDE) SOAP MEIJER ANTIBACTERIAL WHITE TEA AND BERRY HAND (BENZALKONIUM CHLORIDE) SOAP [MEIJER, INC.] 1 Current NDC, 2 package rows 20250529_35bbdd67-6d15-26b6-e063-6394a90a3f96.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.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 79481-0125-1 79481012501 1650 mL in 1 BOTTLE (79481-0125-1) 1650 ml 2024-12-05 No No Current