Drug Facts

Active ingredient

Magnesium Oxide 400 mg

(241.3 mg Elemental Magnesium)

Purpose

Antacid

relieves: ■ acid indigestion ■ upset stomach

you have kidney disease
you are taking a prescription drug (antacids may interact with certain prescription drugs)
you are pregnant or breast feeding.

Do not take more than 2 tablets in a 24 hour period.

take one or two antacid tablets daily. Do not exceed two tablets unless directed by a physician.

Store at controlled room temperature 15° to 30°C (59° to 86°F).
Tamper evident, do not use if imprinted safety seal under cap is broken or missing.

Croscarmellose Sodium, Microcrystalline Cellulose, Silicon Dioxide, and Stearic Acid.

Call Method at 1-877-250-3427 or FDA at 1-800-FDA-1088

Manufactured for:
Method Pharmaceuticals, LLC
Fort Worth, Texas 76118

Rev. 04/18

NDC: 71335-1960-1: 60 Tablets in a BOTTLE

NDC: 71335-1960-2: 30 Tablets in a BOTTLE

NDC: 71335-1960-3: 90 Tablets in a BOTTLE

NDC: 71335-1960-4: 100 Tablets in a BOTTLE

NDC: 71335-1960-5: 120 Tablets in a BOTTLE

Magnesium Oxide 400 mg Tablet

MAGNESIUM OXIDE
magnesium oxide tablet

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
MAGNESIUM OXIDE (UNII: 3A3U0GI71G) (MAGNESIUM CATION - UNII:T6V3LHY838)	MAGNESIUM OXIDE	400 mg

Ingredient Name	Strength
Inactive Ingredients
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
STEARIC ACID (UNII: 4ELV7Z65AP)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:71335-1960-1	60 in 1 BOTTLE; Type 0: Not a Combination Product	10/06/2021
2	NDC:71335-1960-2	30 in 1 BOTTLE; Type 0: Not a Combination Product	10/06/2021
3	NDC:71335-1960-3	90 in 1 BOTTLE; Type 0: Not a Combination Product	10/06/2021
4	NDC:71335-1960-4	100 in 1 BOTTLE; Type 0: Not a Combination Product	10/06/2021
5	NDC:71335-1960-5	120 in 1 BOTTLE; Type 0: Not a Combination Product	10/06/2021

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M001	07/25/2018

Labeler - Bryant Ranch Prepack (171714327)

Registrant - Bryant Ranch Prepack (171714327)

Name	Address	ID/FEI	Business Operations
Establishment
Bryant Ranch Prepack		171714327	REPACK(71335-1960) , RELABEL(71335-1960)