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NDC 41167-1004-05 Rolaids Ultra Strength Fruit 1000; 200 mg/1; mg/1 Details

Rolaids Ultra Strength Fruit 1000; 200 mg/1; mg/1

Rolaids Ultra Strength Fruit is a ORAL TABLET, CHEWABLE in the HUMAN OTC DRUG category. It is labeled and distributed by Chattem, Inc.. The primary component is CALCIUM CARBONATE; MAGNESIUM HYDROXIDE.

MedlinePlus Drug Summary

Calcium carbonate is a dietary supplement used when the amount of calcium taken in the diet is not enough. Calcium is needed by the body for healthy bones, muscles, nervous system, and heart. Calcium carbonate also is used as an antacid to relieve heartburn, acid indigestion, and upset stomach. It is available with or without a prescription. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.

Related Packages: 41167-1004-05
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Calcium Carbonate

Magnesium hydroxide is used to treat occasional constipation in children and adults on a short-term basis. Magnesium hydroxide is in a class of medications called saline laxatives. It works by causing water to be retained with the stool. This increases the number of bowel movements and softens the stool so it is easier to pass.

Related Packages: 41167-1004-05
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Magnesium Hydroxide

Product Information

NDC	41167-1004
Product ID	41167-1004_cc08b1ec-6999-438b-b5df-492e99c7480c
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	Rolaids Ultra Strength Fruit
Proprietary Name Suffix	n/a
Non-Proprietary Name	Calcium carbonate and Magnesium hydroxide
Product Type	HUMAN OTC DRUG
Dosage Form	TABLET, CHEWABLE
Route	ORAL
Active Ingredient Strength	1000; 200
Active Ingredient Units	mg/1; mg/1
Substance Name	CALCIUM CARBONATE; MAGNESIUM HYDROXIDE
Labeler Name	Chattem, Inc.
Pharmaceutical Class	Blood Coagulation Factor [EPC], Calcium [CS], Calculi Dissolution Agent [EPC], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhi
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH DRUG
Application Number	M001
Listing Certified Through	2024-12-31

Package

NDC 41167-1004-05 (41167100405)

Pricing Information	N/A
NDC Package Code	41167-1004-5
Billing NDC	41167100405
Package	3 PACKAGE in 1 CELLO PACK (41167-1004-5) / 10 TABLET, CHEWABLE in 1 PACKAGE (41167-1004-4)
Marketing Start Date	2013-09-01
NDC Exclude Flag	N