Aarica
- Product NDC
- 54633-101
- 11-digit product format
- 546330101
- Labeler code
- 54633
- Product ID
- 54633-101_97b770e7-9125-4db8-89ee-f1b66e01a755
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aluminum Chloride
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- The Podiatree Co
- Application
- part350
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2014-05-06
- Marketing end
- 0000-00-00
- Substance
- ALUMINUM CHLORIDE
- Active strength
- 15 g/100mL
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 54633-101-12 | Aarica | 88.72 mL in 1 BOTTLE | LIQUID | 88.72 | | 2 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 54633-101 | AARICA (ALUMINUM CHLORIDE) LIQUID [THE PODIATREE CO] | 2 | Legacy NDC, 1 package rows | 20140508_ed6028cb-4f23-40b8-bcb2-2487dd4a4526.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 54633-101-12 | 54633010112 | 88.72 mL in 1 BOTTLE | 88.72 ml | Historical |