MINTOX MAXIMUM STRENGTH
- Product NDC
- 71205-515
- 11-digit product format
- 712050515
- Labeler code
- 71205
- Product ID
- 71205-515_dddf9006-4715-487a-b12f-67d56a9e1993
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- aluminum hydroxide, magnesium hydroxide, dimethicone
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- Proficient Rx LP
- 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#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71205-515-35 | MINTOX MAXIMUM STRENGTH | 355 mL in 1 BOTTLE | SUSPENSION | 355 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71205-515 | MINTOX MAXIMUM STRENGTH (ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE) SUSPENSION [PROFICIENT RX LP] | 4 | Current NDC, Legacy NDC, 1 package rows | 20231111_b7711b50-c14a-44d6-b647-1f31284f87ea.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 |
|---|
| 71205-515-35 | 71205051535 | 355 mL in 1 BOTTLE (71205-515-35) | 355 ml | 2020-12-16 | 0000-00-00 | No | No | Current |