Label: MAGNESIUM OXIDE tablet
- NDC Code(s): 54738-974-01
- Packager: Richmond Pharmaceuticals, Inc.
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Updated August 24, 2019
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- ACTIVE INGREDIENT (In each tablet)
Ask a doctor or pharmacist before use if you are:
taking a prescription drug. Antacids may interact with certain prescription drugs.
Do not take
more than 2 tablets in a 24 hour period or use the maximum dosage of this product for more than two weeks, except under the advise and supervision of a physician. May have a laxative effect.
- OTHER INFORMATION
- INACTIVE INGREDIENTS
- Questions or Comments
- PRINCIPAL DISPLAY PANEL
INGREDIENTS AND APPEARANCE
magnesium oxide tablet
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:54738-974 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MAGNESIUM OXIDE (UNII: 3A3U0GI71G) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM OXIDE 420 mg Inactive Ingredients Ingredient Name Strength CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U) MAGNESIUM STEARATE (UNII: 70097M6I30) Product Characteristics Color white (Off) Score no score Shape ROUND Size 12mm Flavor Imprint Code AP;137 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:54738-974-01 100 in 1 BOTTLE; Type 0: Not a Combination Product 02/01/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part331 02/01/2016 Labeler - Richmond Pharmaceuticals, Inc. (043569607) Registrant - Advance Pharmaceutical, Inc (078301063) Establishment Name Address ID/FEI Business Operations Advance Pharmaceutical, Inc 078301063 manufacture(54738-974)