Home NDC 84540-323-01 Ki No Sin
Product NDC 84540-323
Requested package NDC 84540-323-01
11-digit product format 845400323
Labeler code 84540
Product ID 84540-323_3d53e002-3a8f-c746-e063-6394a90a11f5
Type HUMAN OTC DRUG
Nonproprietary name Calcium Carbonate
Dosage form CAPSULE
Route ORAL
Labeler NPG Bio Pharmaceuticals Co.,Ltd.
Application M022
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-08-29
Substance CALCIUM CARBONATE
Active strength 55 mg/500mg
Pharmacologic classes Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Ki No Sin
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CALCIUM CARBONATE 55 mg/500mg
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination H0G9379FGK Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 84540-323-01 Ki No Sin 500 mg in 1 BOTTLE, PLASTIC CAPSULE 500 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 84540-323 KI NO SIN (CALCIUM CARBONATE) CAPSULE [NPG BIO PHARMACEUTICALS CO.,LTD.] 4 Current NDC, 1 package rows 20241223_20cf8f80-c638-4d94-e063-6294a90a5400.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 31 of 39 · 779 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Topicale BENZOCAINE Medical Products Laboratories, Inc. 8282a4a6-b77c-75fc-e053-2991aa0ad4ac 2024-12-16 Warnings Exact identifier application number: M022 Topicale Xtra BENZOCAINE Medical Products Laboratories,Inc. 9452bff4-8c08-eff9-e053-2a95a90a67ed 2024-12-16 Warnings Exact identifier application number: M022 PHENOL PHENOL CHAIN DRUG MARKETING ASSOCIATION INC. 2379e23a-72fe-4e94-9d7e-9b623c0db174 2024-12-13 Warnings Exact identifier application number: M022 KANKA SoftBrush BENZOCAINE AND ZINC CHLORIDE Blistex Inc 093f3545-1d8e-48a3-a533-e9c3ae6d740b 2024-12-12 Warnings Exact identifier application number: M022 Topicale BENZOCAINE Medical Products Laboratories, Inc. 826eaef8-4457-3dc2-e053-2991aa0a528b 2024-12-11 Warnings Exact identifier application number: M022 Topicale BENZOCAINE Medical Products Laboratories, Inc. 8281700c-10f9-841c-e053-2991aa0a918f 2024-12-11 Warnings Exact identifier application number: M022 Topicale BENZOCAINE Medical Products Laboratories, Inc. 82824416-80de-76bd-e053-2a91aa0ad8b5 2024-12-11 Warnings Exact identifier application number: M022 Topicale Xtra BENZOCAINE Medical Products Laboratories,Inc. e3da0e63-a891-72bd-e053-2a95a90a58bc 2024-12-11 Warnings Exact identifier application number: M022 Topicale Xtra BENZOCAINE Medical Products Laboratories, Inc. e3d924b5-0788-46d3-e053-2995a90a027b 2024-12-11 Warnings Exact identifier application number: M022 Fluoride Bits SODIUM MONOFLUOROPHOSPHATE 0.76% The Kind Lab, Inc. fa433031-7376-0e5b-e053-6394a90a5f75 2024-12-11 Warnings Exact identifier application number: M022 Fluoride Bits SODIUM MONOFLUOROPHOSPHATE 0.76% The Kind Lab, Inc. eedf13dc-a009-027a-e053-2995a90a8ec8 2024-12-11 Warnings Exact identifier application number: M022 NATURAL LEMON MINT HERB THROAT DROPS MENTHOL Ricola USA Inc. 763e8234-60be-4b1f-9f78-01c574f35d0a 2024-12-10 Warnings Exact identifier application number: M022 Natural Cherry Honey Herb Throat Drops MENTHOL Ricola USA Inc. 989f8509-cd28-48e7-9aa1-baddfbcac95a 2024-12-10 Warnings Exact identifier application number: M022 ORGANIC PEPPERMINT HERB THROAT DROPS MENTHOL Ricola USA Inc. f75c8967-40e6-473a-b403-941354cb0be1 2024-12-10 Warnings Exact identifier application number: M022 Natural Cherry Honey Herb Throat Drops MENTHOL Ricola USA Inc. c56be34d-1dd5-4200-9723-3a73180cb759 2024-12-10 Warnings Exact identifier application number: M022 Cherry Throat Drops MENTHOL Ricola USA Inc. 89257ceb-af0f-4516-88f7-6dfdab9e14f4 2024-12-10 Warnings Exact identifier application number: M022 BERRY MEDLEY THROAT DROPS MENTHOL Ricola USA Inc. 9bfd2ea7-745b-47f8-bd8a-9dbeeaad8b95 2024-12-10 Warnings Exact identifier application number: M022 NATURAL LEMON MINT HERB THROAT DROPS MENTHOL Ricola USA Inc. 6a81e5c7-834d-44da-853f-8f6103236311 2024-12-10 Warnings Exact identifier application number: M022 SUGAR FREE SWISS CHERRY HERB THROAT DROPS MENTHOL Ricola USA Inc. 8a24f614-8e21-4ab2-8c0e-6af947911ccd 2024-12-10 Warnings Exact identifier application number: M022 RICOLA MAX NASAL CARE COOL MENTHOL MENTHOL Ricola USA Inc. a2e189a2-65ae-48a9-99ad-8795334082df 2024-12-10 Warnings Exact identifier application number: M022
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 84540-323-01 84540032301 500 mg in 1 BOTTLE, PLASTIC (84540-323-01) 500 mg 2024-08-29 No No Current