rite aid ultra strength assorted berries

Generic: calcium carbonate

Labeler: rite aid corporation
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name rite aid ultra strength assorted berries
Generic Name calcium carbonate
Labeler rite aid corporation
Dosage Form TABLET, CHEWABLE
Routes
ORAL
Active Ingredients

calcium carbonate 1000 mg/1

Manufacturer
RITE AID CORPORATION

Identifiers & Regulatory

Product NDC 11822-1037
Product ID 11822-1037_ee63f4ae-cad5-4094-a012-2daa98c0ccef
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M001
Listing Expiration 2026-12-31
Marketing Start 2019-03-20

Pharmacologic Class

Classes
blood coagulation factor [epc] calcium [cs] cations divalent [cs] increased coagulation factor activity [pe] phosphate binder [epc] phosphate chelating activity [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 118221037
Hyphenated Format 11822-1037

Supplemental Identifiers

RxCUI
308892
UPC
0011822706278
UNII
H0G9379FGK

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 rite aid ultra strength assorted berries (source: ndc)
Generic Name calcium carbonate (source: ndc)
Application Number M001 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1000 mg/1
source: ndc
Packaging
  • 160 TABLET, CHEWABLE in 1 BOTTLE (11822-1037-1)
  • 72 TABLET, CHEWABLE in 1 BOTTLE (11822-1037-2)
source: ndc

Packages (2)

11822-1037-1 160 TABLET, CHEWABLE in 1 BOTTLE (11822-1037-1) 11822-1037-2 72 TABLET, CHEWABLE in 1 BOTTLE (11822-1037-2)

Ingredients (1)

calcium carbonate (1000 mg/1)

Linked Drug Pages (1)

Rite Aid Ultra Strength Assorted Berries ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "ee63f4ae-cad5-4094-a012-2daa98c0ccef", "openfda": {"upc": ["0011822706278"], "unii": ["H0G9379FGK"], "rxcui": ["308892"], "spl_set_id": ["ea918cb1-af3e-4a02-bd34-db4ad1b0e6bd"], "manufacturer_name": ["RITE AID CORPORATION"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "160 TABLET, CHEWABLE in 1 BOTTLE (11822-1037-1)", "package_ndc": "11822-1037-1", "marketing_start_date": "20190320"}, {"sample": false, "description": "72 TABLET, CHEWABLE in 1 BOTTLE (11822-1037-2)", "package_ndc": "11822-1037-2", "marketing_start_date": "20190320"}], "brand_name": "Rite Aid Ultra Strength Assorted Berries", "product_id": "11822-1037_ee63f4ae-cad5-4094-a012-2daa98c0ccef", "dosage_form": "TABLET, CHEWABLE", "pharm_class": ["Blood Coagulation Factor [EPC]", "Calcium [CS]", "Cations", "Divalent [CS]", "Increased Coagulation Factor Activity [PE]", "Phosphate Binder [EPC]", "Phosphate Chelating Activity [MoA]"], "product_ndc": "11822-1037", "generic_name": "Calcium Carbonate", "labeler_name": "RITE AID CORPORATION", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Rite Aid Ultra Strength", "brand_name_suffix": "Assorted Berries", "active_ingredients": [{"name": "CALCIUM CARBONATE", "strength": "1000 mg/1"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190320", "listing_expiration_date": "20261231"}