multi symptom antacid

Generic: calcium carbonate ,magnesium hydroxide,simethicone

Labeler: discount drug mart
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name multi symptom antacid
Generic Name calcium carbonate ,magnesium hydroxide,simethicone
Labeler discount drug mart
Dosage Form TABLET, CHEWABLE
Routes
ORAL
Active Ingredients

calcium carbonate 675 mg/1, dimethicone, unspecified 60 mg/1, magnesium hydroxide 135 mg/1

Manufacturer
DISCOUNT DRUG MART

Identifiers & Regulatory

Product NDC 53943-107
Product ID 53943-107_3e835724-4898-430c-e063-6294a90a5abe
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M001
Listing Expiration 2026-12-31
Marketing Start 2019-05-15

Pharmacologic Class

Classes
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] inhibition small intestine fluid/electrolyte absorption [pe] magnesium ion exchange activity [moa] osmotic activity [moa] osmotic laxative [epc] phosphate binder [epc] phosphate chelating activity [moa] skin barrier activity [pe] stimulation large intestine fluid/electrolyte secretion [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 53943107
Hyphenated Format 53943-107

Supplemental Identifiers

RxCUI
476553
UNII
H0G9379FGK 92RU3N3Y1O NBZ3QY004S

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name multi symptom antacid (source: ndc)
Generic Name calcium carbonate ,magnesium hydroxide,simethicone (source: ndc)
Application Number M001 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 675 mg/1
  • 60 mg/1
  • 135 mg/1
source: ndc
Packaging
  • 100 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (53943-107-10)
source: ndc

Packages (1)

53943-107-10 100 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (53943-107-10)

Ingredients (3)

calcium carbonate (675 mg/1) dimethicone, unspecified (60 mg/1) magnesium hydroxide (135 mg/1)

Linked Drug Pages (1)

Multi Symptom Antacid ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3e835724-4898-430c-e063-6294a90a5abe", "openfda": {"unii": ["H0G9379FGK", "92RU3N3Y1O", "NBZ3QY004S"], "rxcui": ["476553"], "spl_set_id": ["c5bae2fb-4625-4eff-b989-000f6b8d9054"], "manufacturer_name": ["DISCOUNT DRUG MART"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (53943-107-10)", "package_ndc": "53943-107-10", "marketing_start_date": "20190515"}], "brand_name": "Multi Symptom Antacid", "product_id": "53943-107_3e835724-4898-430c-e063-6294a90a5abe", "dosage_form": "TABLET, CHEWABLE", "pharm_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]", "Inhibition Small Intestine Fluid/Electrolyte Absorption [PE]", "Magnesium Ion Exchange Activity [MoA]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Phosphate Binder [EPC]", "Phosphate Chelating Activity [MoA]", "Skin Barrier Activity [PE]", "Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]"], "product_ndc": "53943-107", "generic_name": "Calcium carbonate ,Magnesium hydroxide,Simethicone", "labeler_name": "DISCOUNT DRUG MART", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Multi Symptom", "brand_name_suffix": "Antacid", "active_ingredients": [{"name": "CALCIUM CARBONATE", "strength": "675 mg/1"}, {"name": "DIMETHICONE, UNSPECIFIED", "strength": "60 mg/1"}, {"name": "MAGNESIUM HYDROXIDE", "strength": "135 mg/1"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190515", "listing_expiration_date": "20261231"}