MINTOX MAXIMUM STRENGTH
- Product NDC
- 68071-4114
- 11-digit product format
- 680714114
- Labeler code
- 68071
- Product ID
- 68071-4114_1a134f90-34cd-3738-e063-6294a90a5eea
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- aluminum hydroxide, magnesium hydroxide, dimethicone
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- M001
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2011-02-01
- Substance
- ALUMINUM HYDROXIDE; DIMETHICONE; MAGNESIUM HYDROXIDE
- Active strength
- 400; 40; 400 mg/5mL; mg/5mL; mg/5mL
- Pharmacologic classes
- Calculi Dissolution Agent [EPC], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Skin Barrier Activity [PE], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- MINTOX MAXIMUM STRENGTH
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALUMINUM HYDROXIDE | 400 mg/5mL |
| DIMETHICONE | 40 mg/5mL |
| MAGNESIUM HYDROXIDE | 400 mg/5mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 5QB0T2IUN0, 92RU3N3Y1O, NBZ3QY004S |
| Rxcui | 237870, 708127 |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68071-4114-1 | MINTOX MAXIMUM STRENGTH | 355 mL in 1 BOTTLE | SUSPENSION | 355 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68071-4114 | MINTOX MAXIMUM STRENGTH (ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE) SUSPENSION [NUCARE PHARMACEUTICALS,INC.] | 5 | Current NDC, Legacy NDC, 1 package rows | 20240606_5b1f4c78-d42e-32c7-e053-2991aa0a1985.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-4114-1 | 68071411401 | 355 mL in 1 BOTTLE (68071-4114-1) | 355 ml | 2017-10-09 | 0000-00-00 | No | No | Current |