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NDC 27854-0117-01 Melox 400; 40; 400 mg/10mL; mg/10mL; mg/10mL Details
Melox 400; 40; 400 mg/10mL; mg/10mL; mg/10mL
Melox is a ORAL LIQUID in the HUMAN OTC DRUG category. It is labeled and distributed by Belmora LLC. The primary component is ALUMINUM HYDROXIDE; DIMETHICONE; MAGNESIUM HYDROXIDE.
MedlinePlus Drug Summary
Aluminum Hydroxide, Magnesium Hydroxide are antacids used together to relieve heartburn, acid indigestion, and upset stomach. They may be used to treat these symptoms in patients with peptic ulcer, gastritis, esophagitis, hiatal hernia, or too much acid in the stomach (gastric hyperacidity). They combine with stomach acid and neutralize it. Aluminum Hydroxide, Magnesium Hydroxide are available without a prescription. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
Related Packages: 27854-0117-01Last Updated: 03/24/2024
MedLinePlus Full Drug Details: Aluminum Hydroxide and Magnesium Hydroxide
Simethicone is used to treat the symptoms of gas such as uncomfortable or painful pressure, fullness, and bloating. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
Related Packages: 27854-0117-01Last Updated: 03/24/2024
MedLinePlus Full Drug Details: Simethicone
Product Information
| NDC | 27854-0117 |
|---|---|
| Product ID | 27854-117_30664d3b-521c-4914-9c59-88688f8f63d4 |
| Associated GPIs | |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | Melox |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Aluminum hydroxide, Magnesium hydroxide, Simethicone |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | LIQUID |
| Route | ORAL |
| Active Ingredient Strength | 400; 40; 400 |
| Active Ingredient Units | mg/10mL; mg/10mL; mg/10mL |
| Substance Name | ALUMINUM HYDROXIDE; DIMETHICONE; MAGNESIUM HYDROXIDE |
| Labeler Name | Belmora LLC |
| Pharmaceutical Class | 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 |
| DEA Schedule | n/a |
| Marketing Category | OTC MONOGRAPH FINAL |
| Application Number | part331 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 27854-0117-01 (27854011701)
| NDC Package Code | 27854-117-01 |
|---|---|
| Billing NDC | 27854011701 |
| Package | 355 mL in 1 BOTTLE (27854-117-01) |
| Marketing Start Date | 2023-05-01 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |