Home NDC 66096-751 Aralia Racemosa MT
Product NDC 66096-751
11-digit product format 660960751
Labeler code 66096
Product ID 66096-751_d43abd50-5ff6-883c-e053-2995a90a5f05
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Aralia Racemosa
Dosage form LIQUID
Route ORAL
Labeler OHM PHARMA INC.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2019-03-01
Substance ARALIA RACEMOSA ROOT
Active strength .25 1/.25L
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Aralia Racemosa MT
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ARALIA RACEMOSA ROOT .25 1/.25L
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination T90W4582DU 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 66096-751-08 Aralia Racemosa MT 0.25 L in 1 BOTTLE LIQUID 0.25 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 66096-751 ARALIA RACEMOSA MT (ARALIA RACEMOSA) LIQUID [OHM PHARMA INC.] 3 Current NDC, Legacy NDC, 1 package rows 20211229_8d94bf34-1ef5-4b94-89a6-a6b65183627d.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 Marketing start Marketing end Sample Exclude flag Status 66096-751-08 66096075108 .25 L in 1 BOTTLE (66096-751-08) 2019-03-01 0000-00-00 No No Current