Home NDC 66096-783 Anacardium Orientale
Product NDC 66096-783
11-digit product format 660960783
Labeler code 66096
Product ID 66096-783_d450927c-8441-efd6-e053-2a95a90a4f4e
Type HUMAN OTC DRUG
Nonproprietary name ANACARDIUM ORIENTALE
Dosage form PELLET
Route ORAL
Labeler OHM PHARMA INC.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2019-11-01
Substance SEMECARPUS ANACARDIUM JUICE
Active strength 6 [hp_C]/6[hp_C]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Anacardium Orientale
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SEMECARPUS ANACARDIUM JUICE 6 [hp_C]/6[hp_C]
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination Y0F0BU8RDU 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 66096-783-01 Anacardium Orientale 6 [hp_C] in 1 TUBE PELLET 6 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 66096-783 ANACARDIUM ORIENTALE PELLET [OHM PHARMA INC.] 3 Current NDC, Legacy NDC, 1 package rows 20211230_97013586-b2af-4cbb-9cd9-5f8bd8702410.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 66096-783-01 66096078301 6 [hp_C] in 1 TUBE (66096-783-01) 2019-11-01 0000-00-00 No No Current