Home NDC 48951-7218 Millefolium 2X
Product NDC 48951-7218
11-digit product format 489517218
Labeler code 48951
Product ID 48951-7218_36eaca5c-9016-cfb4-e063-6294a90a325c
Type HUMAN OTC DRUG
Nonproprietary name Millefolium 2X
Dosage form LIQUID
Route ORAL
Labeler Uriel Pharmacy, Inc
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance ACHILLEA MILLEFOLIUM
Active strength 2 [hp_X]/mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Millefolium 2X
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ACHILLEA MILLEFOLIUM 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 2FXJ6SW4PK 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 48951-7218-3 Millefolium 2X 60 mL in 1 BOTTLE, DROPPER LIQUID 60 1
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 48951-7218-3 48951721803 60 mL in 1 BOTTLE, DROPPER (48951-7218-3) 60 ml 2009-09-01 No No Current