Home NDC 41250-860 Meijer Ear Relief Ear Drops
Product NDC 41250-860
11-digit product format 412500860
Labeler code 41250
Product ID 41250-860_2f39ceb6-bf78-73b8-e063-6394a90a8397
Type HUMAN OTC DRUG
Nonproprietary name CHAMOMILE, MERCURIUS SOLUBILIS, SULFUR
Dosage form SOLUTION/ DROPS
Route AURICULAR (OTIC)
Labeler Meijer Distribution Inc
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-10-01
Substance MATRICARIA CHAMOMILLA; MERCURIUS SOLUBILIS; SULFUR
Active strength 10; 15; 12 [hp_X]/12mL; [hp_X]/12mL; [hp_X]/12mL
NDC exclude flag No
Listing certified through 2026-12-31
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 Ear Relief Ear Drops
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MATRICARIA CHAMOMILLA 10 [hp_X]/12mL MERCURIUS SOLUBILIS 15 [hp_X]/12mL SULFUR 12 [hp_X]/12mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination G0R4UBI2ZZ Internal UNII lookup 324Y4038G2 Internal UNII lookup 70FD1KFU70 Internal UNII 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 41250-860-07 Meijer Ear Relief Ear Drops 12 mL in 1 BOTTLE SOLUTION/ DROPS 12 3 41250-860-07 Meijer Ear Relief Ear Drops 1 in 1 BOX SOLUTION/ DROPS 1 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 41250-860 MEIJER EAR RELIEF EAR DROPS (CHAMOMILE, MERCURIUS SOLUBILIS, SULFUR) SOLUTION/ DROPS [MEIJER DISTRIBUTION INC] 3 Current NDC, Legacy NDC, 2 package rows 20250303_8ff0fa61-964e-77a8-e053-2a95a90a2d3a.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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 41250-860-07 41250086007 1 BOTTLE in 1 BOX (41250-860-07) / 12 mL in 1 BOTTLE 1 bottle 2009-10-01 0000-00-00 No No Current