ProCure DryDrox
- Product NDC
- 55681-031
- 11-digit product format
- 556810031
- Labeler code
- 55681
- Product ID
- 55681-031_3ab4efb6-bd31-2583-e063-6294a90a415b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aluminum Hydroxide Gel 2%
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Twin Med LLC
- Application
- M016
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-09-15
- Substance
- ALUMINUM HYDROXIDE
- Active strength
- 2 g/100g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- ProCure DryDrox
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALUMINUM HYDROXIDE | 2 g/100g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 5QB0T2IUN0 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 55681-031-04 | ProCure DryDrox | 106 g in 1 TUBE | OINTMENT | 106 | | 1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 55681-031-04 | 55681003104 | 106 g in 1 TUBE (55681-031-04) | 106 g | 2025-09-15 | No | No | Current |