Home NDC 48951-6085 Koromiko 2X
Product NDC 48951-6085
11-digit product format 489516085
Labeler code 48951
Product ID 48951-6085_58b7ffcf-b913-377f-e063-6294a90adb7f
Type HUMAN OTC DRUG
Nonproprietary name Koromiko 2X
Dosage form LIQUID
Route ORAL
Labeler Uriel Pharmacy, Inc
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance HEIMIA SALICIFOLIA LEAF
Active strength 2 [hp_X]/mL
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 Koromiko 2X
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HEIMIA SALICIFOLIA LEAF 2 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 0K96FZ8ZI2 Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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 Sample Exclude flag Status 48951-6085-3 48951608503 60 mL in 1 BOTTLE, DROPPER (48951-6085-3) 60 ml 2009-09-01 No No Current