Home NDC 0220-0189 Aloe
Product NDC 0220-0189
11-digit product format 002200189
Labeler code 0220
Product ID 0220-0189_0051c7de-8a83-0905-e063-6294a90a0bec
Type HUMAN OTC DRUG
Nonproprietary name ALOE FEROX LEAF
Dosage form PELLET
Route ORAL
Labeler Boiron
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 1983-03-03
Substance ALOE FEROX LEAF
Active strength 5 [hp_C]/5[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 Aloe
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALOE FEROX LEAF 5 [hp_C]/5[hp_C]
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 0D145J8EME 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 0220-0189-41 Aloe 5 [hp_C] in 1 TUBE PELLET 5 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0220-0189 ALOE (ALOE FEROX LEAF ) PELLET [BOIRON] 3 Current NDC, Legacy NDC, 1 package rows 20230713_83ec2bea-a05a-558d-e053-2991aa0a56f6.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 0220-0189-41 00220018941 5 [hp_C] in 1 TUBE (0220-0189-41) 1983-03-03 0000-00-00 No No Current