Home NDC 21130-021 Fiber Caplets
Product NDC 21130-021
11-digit product format 211300021
Labeler code 21130
Product ID 21130-021_424a8a8a-5774-a6d9-e063-6294a90a4a41
Type HUMAN OTC DRUG
Nonproprietary name Calcium Polycarbophil
Dosage form TABLET, FILM COATED
Route ORAL
Labeler SAFEWAY
Application M007
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-10-02
Substance CALCIUM POLYCARBOPHIL
Active strength 625 mg/1
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 Fiber Caplets
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CALCIUM POLYCARBOPHIL 625 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 8F049NKY49 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 308934 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 21130-021-40 Fiber Caplets 140 in 1 BOTTLE TABLET, FILM COATED 140 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 21130-021 FIBER CAPLETS (CALCIUM POLYCARBOPHIL) TABLET, FILM COATED [SAFEWAY] 5 Current NDC, Legacy NDC, 1 package rows 20241105_08e2e8b0-90b3-48d6-a72a-40688c74771a.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 42 · 833 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Rite Aid Stool Softener DOCUSATE CALCIUM Rite Aid 281b2bc7-4980-4205-a33f-cb1974af8d06 2024-12-18 Warnings Exact identifier application number: M007 Topcare Stool Softener DOCUSATE SODIUM TOPCO ASSOCIATES LLC 93158bd3-c830-4b12-ab1c-133a4bdb9c78 2024-12-18 Warnings Exact identifier application number: M007 HEB Stool Softener DOCUSATE SODIUM H E B afc54b8e-03d9-418c-9322-97d68f929031 2024-12-18 Warnings Exact identifier application number: M007 Foster and Thrive Gentle Laxative BISACODYL Strategic Sourcing Services LLC d03c2c42-d9d9-4b4b-a6ae-31d99425a228 2024-12-18 Warnings Exact identifier application number: M007 EX-LAX REGULAR STRENGTH CHOCOLATED STIMULANT LAXATIVE SENNOSIDES Haleon US Holdings LLC 59a26a7f-516f-4507-8dec-f40cf6cfaffc 2024-12-17 Warnings Exact identifier application number: M007 EX-LAX MAXIMUM STRENGTH STIMULANT LAXATIVE SENNOSIDES Haleon US Holdings LLC fb170340-c996-46cf-b165-84e136ba4151 2024-12-17 Warnings Exact identifier application number: M007 Senna Syrup NATURAL VEGETABLE LAXATIVE Bryant Ranch Prepack 7d1f092e-0e5b-4fed-a095-64449751582d 2024-12-16 Warnings Exact identifier application number: M007 Drug Mart Vegetable Laxative plus Stool Softener DOCUSATE SODIUM, SENNOSIDES Discount Drug Mart, Inc 1b6d59e8-112f-447f-b6e9-526b7d3bd01e 2024-12-13 Warnings Exact identifier application number: M007 Drug Mart Stool Softener plus Stimulant Laxative DOCUSATE SODIUM, SENNOSIDES Discount Drug Mart, Inc caf74258-922c-4b69-9bd6-57b3e918c7a6 2024-12-13 Warnings Exact identifier application number: M007 Docusate Sodium DOCUSATE SODIUM National Vitamin Company 0c66642c-82cb-42cd-82bb-5f95852cc5d1 2024-12-12 Warnings Exact identifier application number: M007 Foster and Thrive Fiber Laxative 147 CALCIUM POLYCARBOPHIL Strategic Sourcing Services LLC 88d341a6-28aa-4a20-bfed-1d5f3106c2ae 2024-12-12 Warnings Exact identifier application number: M007 Pedia-Lax SODIUM PHOSPHATE, DIBASIC AND SODIUM PHOSPHATE, MONOBASIC C.B. Fleet Company, Inc. f001a37d-8ed4-428b-af12-d6a83c22c127 2024-12-12 Warnings Exact identifier application number: M007 Careone Milk of magnesia Original Milk of Magnesia Original MAGNESIUM HYDROXIDE Retail Business Services, LLC. 13ffb00b-7c6f-47aa-bc82-2402d121a758 2024-12-11 Warnings Exact identifier application number: M007 CareOne Milk of Magnesia Cherry MAGNESIUM HYDROXIDE Retail Business Services, LLC. 1822f90d-f693-48d7-b338-a3f2ddfac4df 2024-12-11 Warnings Exact identifier application number: M007 MILK OF MAGNESIA MINT MAGNESIUM HYDROXIDE GOOD SENSE a951b6d0-9182-e1bc-e053-2a95a90a12b1 2024-12-09 Warnings Exact identifier application number: M007 Sennosides SENNOSIDES Major Pharmaceuticals df3b431b-a1ad-91dd-e053-2995a90aa02f 2024-12-06 Warnings Exact identifier application number: M007 milk of magnesia MAGNESIUM HYDROXIDE CVS Pharmacy b3a36251-edd6-4201-8da1-85d7a6ede173 2024-12-05 Warnings Exact identifier application number: M007 CITRUCEL METHYLCELLULOSE Haleon US Holdings LLC d27f6742-2dcc-451e-b803-6ffe183038ec 2024-12-05 Warnings Exact identifier application number: M007 Laxacin DOCUSATE SODIUM AND SENNOSIDES Alexso, Inc 0df9abaf-3997-4dde-8003-ae3d8d07cf39 2024-12-04 Warnings Exact identifier application number: M007 NuValu Epsom Salt MAGNESIUM SULFATE (HEPTAHYDRATE) J C SALES 9f3cf9a4-e5c0-41ff-9fd3-63efb0d973cd 2024-12-04 Warnings Exact identifier application number: M007
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 21130-021-40 21130002140 140 TABLET, FILM COATED in 1 BOTTLE (21130-021-40) 2020-10-02 0000-00-00 No No Current