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 6 [hp_C]/6[hp_C]
Manufacturer
Identifiers & Regulatory
Product NDC
0220-0190
Product ID
0220-0190_0051d268-8f32-5d6e-e063-6394a90a01e2
Product Type
HUMAN OTC DRUG
Marketing Category
UNAPPROVED HOMEOPATHIC
Listing Expiration
2026-12-31
Marketing Start
1983-03-03
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
02200190
Hyphenated Format
0220-0190
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
- 6 [hp_C]/6[hp_C]
Packaging
- 6 [hp_C] in 1 TUBE (0220-0190-41)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0051d268-8f32-5d6e-e063-6394a90a01e2", "openfda": {"unii": ["0D145J8EME"], "spl_set_id": ["83ec645b-ae8e-5979-e053-2991aa0a554f"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 [hp_C] in 1 TUBE (0220-0190-41)", "package_ndc": "0220-0190-41", "marketing_start_date": "19830303"}], "brand_name": "Aloe", "product_id": "0220-0190_0051d268-8f32-5d6e-e063-6394a90a01e2", "dosage_form": "PELLET", "product_ndc": "0220-0190", "generic_name": "ALOE FEROX LEAF", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Aloe", "active_ingredients": [{"name": "ALOE FEROX LEAF", "strength": "6 [hp_C]/6[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}