Search by Drug Name or NDC

NDC 00536-1293-83 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 Rugby Laboratories. 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: 00536-1293-83
Last Updated: 11/30/2022
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: 00536-1293-83
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Simethicone

Product Information

NDC	00536-1293
Product ID	0536-1293_ec4ea84e-ce4c-4acd-b306-75df725abd6d
Associated GPIs	48991003101810
GCN Sequence Number	002701
GCN Sequence Number Description	mag hydrox/aluminum hyd/simeth ORAL SUSP 200-200-20 ORAL
HIC3	D4B
HIC3 Description	ANTACIDS
GCN	63910
HICL Sequence Number	001168
HICL Sequence Number Description	MAGNESIUM HYDROXIDE/ALUMINUM HYDROXIDE/SIMETHICONE
Brand/Generic	Brand
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	Rugby Laboratories
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 00536-1293-83 (00536129383)

Pricing Information
NDC Package Code	0536-1293-83
Billing NDC	00536129383
Package	355 mL in 1 BOTTLE (0536-1293-83)
Marketing Start Date	2021-06-02
NDC Exclude Flag	N
Price Per Unit	0.011
Pricing Unit	ML
Effective Date	2024-02-21
NDC Description	ANTACID-ANTIGAS LIQUID
Pharmacy Type Indicator	C/I
OTC	Y
Explanation Code	1, 5
Classification for Rate Setting	G
As of Date	2024-02-21

This pricing file, entitled the NADAC (National Average Drug Acquisition Cost) files, provide state Medicaid agencies with covered outpatient drug prices by averaging survey invoice prices from retail community pharmacies across the United States. These pharmacies include independent retail community pharmacies and chain pharmacies. The prices are updated on a weekly and monthly basis

Standard Product Labeling (SPL)/Prescribing Information SPL bd58baac-5790-455a-9c77-236680992579 Details

ACTIVE INGREDIENTS (in each 10 mL )

Aluminum hydroxide (equiv. to dried gel, USP) 400 mg

Magnesium hydroxide 400 mg

Simethicone 40 mg

PURPOSE

Antacid

Antacid

Antigas

USE(S)

relieves:

acid indigestion
heartburn
sour stomach
upset stomach and gas associated with these symptoms

WARNINGS

Do not take more than 80 mL in a 24-hour period, or use the maximum dosage of this product for more than 2 weeks, except under the advice and supervision of a doctor.

ASK A DOCTOR BEFORE USE IF YOU HAVE

kidney disease
a magnesium-restricted diet

ASK A DOCTOR OR PHARMACIST BEFORE USE IF YOU ARE

presently taking a prescription drug. Antacids may interact with certain prescription drugs.

STOP USE AND ASK DOCTOR

if symptoms last more than two weeks

KEEP OUT OF REACH OF CHILDREN

DIRECTIONS

shake well before use
mL = milliliter
adults and children 12 years and older: take 10 mL to 20 mL four times a day, or as directed by a doctor
children under 12 years: consult a doctor

OTHER INFORMATION

each 10 mL contains: magnesium 170 mg, sodium 5 mg
store at controlled room temperature 20ºC-25ºC (68º-77ºF)
do not freeze

INACTIVE INGREDIENTS

ethyl alcohol, flavor, glycerin, hydroxyethyl cellulose, methylparaben, propylene glycol, propylparaben, purified water, saccharin sodium, simethicone emulsion, sorbitol

PRINCIPAL DISPLAY PANEL

Rugby

NDC 0536-1293-83

Regular Strength

Antacid Liquid

Aluminum hydroxide, 400 mg

Magnesium hydroxide, 400 mg

Simethicone, 40 mg

Antacid and Antigas

Original Flavor

Relief of:

Heartburn

Acid Indigestion

Sour Stomach

Pressure & Bloating

12 FL OZ (355 mL)

Alcohol content 0.2% v/v

INGREDIENTS AND APPEARANCE

ANTACID

aluminum hydroxide, magnesium hydroxide, simethicone liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:0536-1293
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) (ALUMINUM HYDROXIDE - UNII:5QB0T2IUN0)	ALUMINUM HYDROXIDE	400 mg in 10 mL
MAGNESIUM HYDROXIDE (UNII: NBZ3QY004S) (MAGNESIUM CATION - UNII:T6V3LHY838)	MAGNESIUM HYDROXIDE	400 mg in 10 mL
DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O)	DIMETHICONE	40 mg in 10 mL

Ingredient Name	Strength
Inactive Ingredients
ALCOHOL (UNII: 3K9958V90M)
GLYCERIN (UNII: PDC6A3C0OX)
HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
WATER (UNII: 059QF0KO0R)
SACCHARIN SODIUM (UNII: SB8ZUX40TY)
SORBITOL (UNII: 506T60A25R)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)

Product Characteristics
Color	WHITE	Score
Shape		Size
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:0536-1293-83	355 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/02/2021

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC MONOGRAPH FINAL	part331	06/02/2021

Labeler - Rugby Laboratories (079246066)

Name	Address	ID/FEI	Business Operations
Establishment
Guardian Drug Company		119210276	MANUFACTURE(0536-1293)

Revised: 6/2021

Document Id: ec4ea84e-ce4c-4acd-b306-75df725abd6d

Set id: bd58baac-5790-455a-9c77-236680992579

Version: 2

Effective Time: 20210602