Aloe
- Product NDC
- 0220-0222
- 11-digit product format
- 002200222
- Labeler code
- 0220
- Product ID
- 0220-0222_227e9fec-6417-d25b-e063-6394a90a08e2
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ALOE FEROX LEAF
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- Boiron
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2024-01-01
- Substance
- ALOE FEROX LEAF
- Active strength
- 200 [kp_C]/200[kp_C]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Matched term |
|---|
| 0D145J8EME | ALOE FEROX LEAF | ALOE FEROX LEAF |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 0220-0222-41 | 00220022241 | 200 [kp_C] in 1 TUBE (0220-0222-41) | 2024-01-01 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Aloe 200CK | Boiron | Boiron, Inc. | 2024-09-19 | HUMAN OTC DRUG LABEL | 1 |