Home NDC 0220-1507 Colocynthis
Product NDC 0220-1507
11-digit product format 002201507
Labeler code 0220
Product ID 0220-1507_f2b86b77-a059-9cf1-e053-2a95a90a099a
Type HUMAN OTC DRUG
Nonproprietary name CITRULLUS COLOCYNTHIS FRUIT PULP
Dosage form PELLET
Route ORAL
Labeler Boiron
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1983-03-03
Substance CITRULLUS COLOCYNTHIS FRUIT PULP
Active strength 30 [hp_C]/30[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 Colocynthis
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CITRULLUS COLOCYNTHIS FRUIT PULP 30 [hp_C]/30[hp_C]
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 23H32AOH17 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 0220-1507-41 Colocynthis 30 [hp_C] in 1 TUBE PELLET 30 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0220-1507 COLOCYNTHIS (CITRULLUS COLOCYNTHIS FRUIT PULP ) PELLET [BOIRON] 2 Current NDC, Legacy NDC, 1 package rows 20230121_854089bc-92f4-38f3-e053-2991aa0a2ca7.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 0220-1507-41 00220150741 30 [hp_C] in 1 TUBE (0220-1507-41) 1983-03-03 0000-00-00 No No Current