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 Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 0D145J8EME |
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 |
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 |