HEARTBURN RELIEF
- Product NDC
- 57896-565
- 11-digit product format
- 578960565
- Labeler code
- 57896
- Product ID
- 57896-565_28d955ae-eec6-64fc-e063-6294a90a154d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- aluminum hydroxide and magnesium carbonate
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- GERI-CARE PHARMACEUTICALS, CORP
- Application
- M001
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-07-01
- Substance
- ALUMINUM HYDROXIDE; MAGNESIUM CARBONATE
- Active strength
- 254; 237.5 mg/5mL; mg/5mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- HEARTBURN RELIEF
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALUMINUM HYDROXIDE | 254 mg/5mL |
| MAGNESIUM CARBONATE | 237.5 mg/5mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 5QB0T2IUN0, 0E53J927NA |
| Rxcui | 245001 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 57896-565-12 | HEARTBURN RELIEF | 355 mL in 1 BOTTLE | SUSPENSION | 355 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 57896-565 | HEARTBURN RELIEF (ALUMINUM HYDROXIDE AND MAGNESIUM CARBONATE) SUSPENSION [GERI-CARE PHARMACEUTICALS, CORP] | 2 | Current NDC, 1 package rows | 20241210_1f1dbf41-cb87-37d4-e063-6394a90ae294.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 57896-565-12 | 57896056512 | 355 mL in 1 BOTTLE (57896-565-12) | 355 ml | 2024-07-01 | No | No | Current |