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NDC 63868-0173-12 Antacid 400; 40; 400 mg/10mL; mg/10mL; mg/10mL Details
Antacid 400; 40; 400 mg/10mL; mg/10mL; mg/10mL
Antacid is a ORAL LIQUID in the HUMAN OTC DRUG category. It is labeled and distributed by Chain Drug Marketing Association Inc.. 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: 63868-0173-12Last Updated: 12/01/2022
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: 63868-0173-12Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Simethicone
Product Information
NDC | 63868-0173 |
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Product ID | 63868-173_d7e6ece9-559a-4090-ac17-d6c936e3bf3f |
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 | Antacid |
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 | Chain Drug Marketing Association Inc. |
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
Package Images

NDC 63868-0173-12 (63868017312)
NDC Package Code | 63868-173-12 |
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Billing NDC | 63868017312 |
Package | 355 mL in 1 BOTTLE (63868-173-12) |
Marketing Start Date | 2022-08-15 |
NDC Exclude Flag | N |
Pricing Information | N/A |
Standard Product Labeling (SPL)/Prescribing Information SPL d7e6ece9-559a-4090-ac17-d6c936e3bf3f Details
ACTIVE INGREDIENTS (in each 10 mL )
USE(S)
WARNINGS
ASK A DOCTOR OR PHARMACIST BEFORE USE IF YOU ARE
DIRECTIONS
OTHER INFORMATION
INACTIVE INGREDIENTS
PRINCIPAL DISPLAY PANEL
INGREDIENTS AND APPEARANCE
ANTACID
aluminum hydroxide, magnesium hydroxide, simethicone liquid |
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Labeler - Chain Drug Marketing Association Inc. (011920774) |