regular strength antacid peppermint

Generic: calcium carbonate

Labeler: akron pharma inc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name regular strength antacid peppermint
Generic Name calcium carbonate
Labeler akron pharma inc
Dosage Form TABLET, CHEWABLE
Routes
ORAL
Active Ingredients

calcium carbonate 500 mg/1

Manufacturer
AKRON PHARMA INC

Identifiers & Regulatory

Product NDC 71399-9940
Product ID 71399-9940_4c1135bf-19aa-7be9-e063-6294a90a97d0
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M001
Listing Expiration 2027-12-31
Marketing Start 2025-09-26

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 713999940
Hyphenated Format 71399-9940

Supplemental Identifiers

RxCUI
308907
UPC
0371399994028
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 regular strength antacid peppermint (source: ndc)
Generic Name calcium carbonate (source: ndc)
Application Number M001 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 150 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (71399-9940-1)
  • 1000 TABLET, CHEWABLE in 1 BOTTLE (71399-9940-2)
source: ndc

Packages (2)

71399-9940-1 150 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (71399-9940-1) 71399-9940-2 1000 TABLET, CHEWABLE in 1 BOTTLE (71399-9940-2)

Ingredients (1)

calcium carbonate (500 mg/1)

Linked Drug Pages (1)

REGULAR STRENGTH ANTACID PEPPERMINT ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4c1135bf-19aa-7be9-e063-6294a90a97d0", "openfda": {"upc": ["0371399994028"], "unii": ["H0G9379FGK"], "rxcui": ["308907"], "spl_set_id": ["3fb78d78-5296-4197-e063-6294a90adaae"], "manufacturer_name": ["AKRON PHARMA INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "150 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (71399-9940-1)", "package_ndc": "71399-9940-1", "marketing_start_date": "20250926"}, {"sample": false, "description": "1000 TABLET, CHEWABLE in 1 BOTTLE (71399-9940-2)", "package_ndc": "71399-9940-2", "marketing_start_date": "20250926"}], "brand_name": "REGULAR STRENGTH ANTACID PEPPERMINT", "product_id": "71399-9940_4c1135bf-19aa-7be9-e063-6294a90a97d0", "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": "71399-9940", "generic_name": "CALCIUM CARBONATE", "labeler_name": "AKRON PHARMA INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "REGULAR STRENGTH ANTACID", "brand_name_suffix": "PEPPERMINT", "active_ingredients": [{"name": "CALCIUM CARBONATE", "strength": "500 mg/1"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250926", "listing_expiration_date": "20271231"}