aloe
Generic: aloe ferox leaf
Labeler: boironDrug Facts
Product Profile
Brand Name
aloe
Generic Name
aloe ferox leaf
Labeler
boiron
Dosage Form
PELLET
Routes
Active Ingredients
aloe ferox leaf 200 [kp_C]/200[kp_C]
Manufacturer
Identifiers & Regulatory
Product NDC
0220-0222
Product ID
0220-0222_227e9fec-6417-d25b-e063-6394a90a08e2
Product Type
HUMAN OTC DRUG
Marketing Category
UNAPPROVED HOMEOPATHIC
Listing Expiration
2026-12-31
Marketing Start
2024-01-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
02200222
Hyphenated Format
0220-0222
Supplemental Identifiers
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
aloe (source: ndc)
Generic Name
aloe ferox leaf (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 200 [kp_C]/200[kp_C]
Packaging
- 200 [kp_C] in 1 TUBE (0220-0222-41)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "227e9fec-6417-d25b-e063-6394a90a08e2", "openfda": {"unii": ["0D145J8EME"], "spl_set_id": ["227e9fec-6416-d25b-e063-6394a90a08e2"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 [kp_C] in 1 TUBE (0220-0222-41)", "package_ndc": "0220-0222-41", "marketing_start_date": "20240101"}], "brand_name": "Aloe", "product_id": "0220-0222_227e9fec-6417-d25b-e063-6394a90a08e2", "dosage_form": "PELLET", "product_ndc": "0220-0222", "generic_name": "ALOE FEROX LEAF", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Aloe", "active_ingredients": [{"name": "ALOE FEROX LEAF", "strength": "200 [kp_C]/200[kp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20240101", "listing_expiration_date": "20261231"}