NDC 50488-0901-01 - Laxacin

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 50488-0901
Requested NDC: 50488-0901-01
Package NDCs from labels: 50488-0901-1, 50488-0901-01
Manufacturer: Advanced Rx Pharmacy of Tennessee, LLC
Effective date: 2024-12-31
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Laxacin - Advanced Rx Pharmacy of Tennessee, LLC	Advanced Rx Pharmacy of Tennessee, LLC	2024-12-31	HUMAN OTC DRUG LABEL
Laxacin - Alexso, Inc	Alexso, Inc	2024-12-04	HUMAN OTC DRUG LABEL
Laxacin - Quality Care Products, LLC	Quality Care Products, LLC	2023-12-21	HUMAN OTC DRUG LABEL
LAXACIN - Direct_Rx	Direct_Rx	2023-10-06	HUMAN OTC DRUG LABEL
Laxacin Laxative Plus Stool Softener	NuCare Pharmaceuticals,Inc.	2021-02-11	HUMAN OTC DRUG LABEL
Laxacin - medsource pharmaceuticals	medsource pharmaceuticals	2018-12-20	HUMAN OTC DRUG LABEL
LAXACIN - DIRECT RX	DIRECT RX	2018-03-26	HUMAN OTC DRUG LABEL
Laxacin Laxative Plus Stool Softener	Dispensing Solutions, Inc. \| PSS World Medical, Inc.	2013-07-12	HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
50488-0901-1	Laxacin	100 in 1 BOTTLE	TABLET	100		8

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
50488-0901	LAXACIN (DOCUSATE SODIUM AND SENNOSIDES) TABLET [ALEXSO, INC]	8	Current NDC, Legacy NDC, 1 package rows	20241208_0df9abaf-3997-4dde-8003-ae3d8d07cf39.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
50488-0901-1	EA - Each	50488-0901	933d71c3-b01d-44ff-b256-0bee20827ae8	1	2012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
DOCUSATE SODIUM	ACTIVE INGREDIENT	F05Q2T2JA0	LAXACIN (DOCUSATE SODIUM AND SENNOSIDES) TABLET [DISPENSING SOLUTIONS, INC.]	2
SENNOSIDES A AND B	ACTIVE INGREDIENT	1B5FPI42EN	LAXACIN (DOCUSATE SODIUM AND SENNOSIDES) TABLET [DISPENSING SOLUTIONS, INC.]	2
DOCUSATE	ACTIVE MOIETY	M7P27195AG	LAXACIN (DOCUSATE SODIUM AND SENNOSIDES) TABLET [DISPENSING SOLUTIONS, INC.]	2
SENNOSIDES A AND B	ACTIVE MOIETY	1B5FPI42EN	LAXACIN (DOCUSATE SODIUM AND SENNOSIDES) TABLET [DISPENSING SOLUTIONS, INC.]	2
ANHYDROUS DIBASIC CALCIUM PHOSPHATE	INACTIVE INGREDIENT	L11K75P92J	LAXACIN (DOCUSATE SODIUM AND SENNOSIDES) TABLET [DISPENSING SOLUTIONS, INC.]	2
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	LAXACIN (DOCUSATE SODIUM AND SENNOSIDES) TABLET [DISPENSING SOLUTIONS, INC.]	2
CROSCARMELLOSE SODIUM	INACTIVE INGREDIENT	M28OL1HH48	LAXACIN (DOCUSATE SODIUM AND SENNOSIDES) TABLET [DISPENSING SOLUTIONS, INC.]	2
D&C YELLOW NO. 10	INACTIVE INGREDIENT	35SW5USQ3G	LAXACIN (DOCUSATE SODIUM AND SENNOSIDES) TABLET [DISPENSING SOLUTIONS, INC.]	2
DEXTROSE	INACTIVE INGREDIENT	IY9XDZ35W2	LAXACIN (DOCUSATE SODIUM AND SENNOSIDES) TABLET [DISPENSING SOLUTIONS, INC.]	2
FD&C YELLOW NO. 6	INACTIVE INGREDIENT	H77VEI93A8	LAXACIN (DOCUSATE SODIUM AND SENNOSIDES) TABLET [DISPENSING SOLUTIONS, INC.]	2
HYPROMELLOSES	INACTIVE INGREDIENT	3NXW29V3WO	LAXACIN (DOCUSATE SODIUM AND SENNOSIDES) TABLET [DISPENSING SOLUTIONS, INC.]	2
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	LAXACIN (DOCUSATE SODIUM AND SENNOSIDES) TABLET [DISPENSING SOLUTIONS, INC.]	2
POLYETHYLENE GLYCOLS	INACTIVE INGREDIENT	3WJQ0SDW1A	LAXACIN (DOCUSATE SODIUM AND SENNOSIDES) TABLET [DISPENSING SOLUTIONS, INC.]	2
SODIUM BENZOATE	INACTIVE INGREDIENT	OJ245FE5EU	LAXACIN (DOCUSATE SODIUM AND SENNOSIDES) TABLET [DISPENSING SOLUTIONS, INC.]	2
STEARIC ACID	INACTIVE INGREDIENT	4ELV7Z65AP	LAXACIN (DOCUSATE SODIUM AND SENNOSIDES) TABLET [DISPENSING SOLUTIONS, INC.]	2
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	LAXACIN (DOCUSATE SODIUM AND SENNOSIDES) TABLET [DISPENSING SOLUTIONS, INC.]	2
DOCUSATE SODIUM	ACTIVE INGREDIENT	F05Q2T2JA0	LAXACIN (DOCUSATE SODIUM AND SENNOSIDES) TABLET [ALEXSO INC]	1
SENNOSIDES A AND B	ACTIVE INGREDIENT	1B5FPI42EN	LAXACIN (DOCUSATE SODIUM AND SENNOSIDES) TABLET [ALEXSO INC]	1
DOCUSATE	ACTIVE MOIETY	M7P27195AG	LAXACIN (DOCUSATE SODIUM AND SENNOSIDES) TABLET [ALEXSO INC]	1
SENNOSIDES	ACTIVE MOIETY	3FYP5M0IJX	LAXACIN (DOCUSATE SODIUM AND SENNOSIDES) TABLET [ALEXSO INC]	1
ANHYDROUS DIBASIC CALCIUM PHOSPHATE	INACTIVE INGREDIENT	L11K75P92J	LAXACIN (DOCUSATE SODIUM AND SENNOSIDES) TABLET [ALEXSO INC]	1
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	LAXACIN (DOCUSATE SODIUM AND SENNOSIDES) TABLET [ALEXSO INC]	1
CROSCARMELLOSE SODIUM	INACTIVE INGREDIENT	M28OL1HH48	LAXACIN (DOCUSATE SODIUM AND SENNOSIDES) TABLET [ALEXSO INC]	1
D&C YELLOW NO. 10	INACTIVE INGREDIENT	35SW5USQ3G	LAXACIN (DOCUSATE SODIUM AND SENNOSIDES) TABLET [ALEXSO INC]	1
DEXTROSE	INACTIVE INGREDIENT	IY9XDZ35W2	LAXACIN (DOCUSATE SODIUM AND SENNOSIDES) TABLET [ALEXSO INC]	1
FD&C YELLOW NO. 6	INACTIVE INGREDIENT	H77VEI93A8	LAXACIN (DOCUSATE SODIUM AND SENNOSIDES) TABLET [ALEXSO INC]	1
HYPROMELLOSES	INACTIVE INGREDIENT	3NXW29V3WO	LAXACIN (DOCUSATE SODIUM AND SENNOSIDES) TABLET [ALEXSO INC]	1
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	LAXACIN (DOCUSATE SODIUM AND SENNOSIDES) TABLET [ALEXSO INC]	1
POLYETHYLENE GLYCOLS	INACTIVE INGREDIENT	3WJQ0SDW1A	LAXACIN (DOCUSATE SODIUM AND SENNOSIDES) TABLET [ALEXSO INC]	1
SODIUM BENZOATE	INACTIVE INGREDIENT	OJ245FE5EU	LAXACIN (DOCUSATE SODIUM AND SENNOSIDES) TABLET [ALEXSO INC]	1
STEARIC ACID	INACTIVE INGREDIENT	4ELV7Z65AP	LAXACIN (DOCUSATE SODIUM AND SENNOSIDES) TABLET [ALEXSO INC]	1
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	LAXACIN (DOCUSATE SODIUM AND SENNOSIDES) TABLET [ALEXSO INC]	1

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 104 of 178 · 3,543 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Tinted Mineral Sunscreen SPF 50	ZINC OXIDE AND TITANIUM DIOXIDE	Topiderm, Inc.	13e5085f-df2b-46b2-b063-e58ce4379905	2025-04-09	Warnings	Exact identifier unii: 15FIX9V2JP
Fiber Laxative	CALCIUM POLYCARBOPHIL	Geri-Care Pharmaceutical Corp	616b4399-7626-5e59-e053-2a91aa0a0f75	2025-04-07	Warnings	Exact identifier application number: M007
Calcium Polycarbophil	CALCIUM POLYCARBOPHIL	CITRAGEN PHARMACEUTICALS, INC.	b23dd90f-ba5a-80fc-e053-2995a90a2286	2025-04-03	Warnings	Exact identifier application number: M007
Phillips Milk Of Magnesia Wild Cherry	PHILLIPS MILK OF MAGNESIA WILD CHERRY	Bayer HealthCare LLC.	0a6d824a-3d9a-07f9-e054-00144ff8d46c	2025-04-01	Warnings	Exact identifier application number: M007
SODIUM PHENYLACETATE and SODIUM BENZOATE	SODIUM PHENYLACETATE AND SODIUM BENZOATE	Ailex Pharmaceuticals, LLC	329655ae-c3c0-46b2-a925-e49777f2076b	2025-03-30	Warnings, Adverse reactions	Exact identifier unii: OJ245FE5EU
ALEX MD PHD Sheer Mineral Sunscreen	ZINC OXIDE, TITANIUM DIOXIDE	PHYSICIAN LABORATORIES INC	8f64c4fa-92ee-4af0-ab1b-6c3673f9a622	2025-03-28	Warnings	Exact identifier unii: 15FIX9V2JP
ALEX MD PHD Tinted Mineral Sunscreen	ZINC OXIDE, TITANIUM DIOXIDE	PHYSICIAN LABORATORIES INC	93873c34-5c72-43c8-b6c2-c65b596191d7	2025-03-28	Warnings	Exact identifier unii: 15FIX9V2JP
City Skin Age Defense Broad Spectrum SPF 50	TITANIUM DIOXIDE AND ZINC OXIDE	Murad, LLC	f8c572a2-b4bc-49e9-95df-359f05bd69b7	2025-03-28	Warnings	Exact identifier unii: 15FIX9V2JP
Bestmade Natural Products BM238	SANTONINE, CINA, SILICEA, INDIGO, AMBROSIA, CUCCURBITA CIT, CUCCURBITA PEP	Bestmade Natural Products	298fb9e2-3f98-01e6-e063-6294a90a7aaf	2025-03-26	Warnings	Exact identifier unii: ETJ7Z6XBU4
it cosmetics Your Skin But Better CC Plus Color Correcting Broad Spectrum SPF 50 Plus Sunscreen Full Coverage Deep FairLight Neutral Tan Rich Honey LightMedium and Neutral Medium	TITANIUM DIOXIDE AND ZINC OXIDE	IT COSMETICS, LLC	e17dc640-30e9-441b-a212-ef1508af7944	2025-03-25	Warnings	Exact identifier unii: 15FIX9V2JP
Bestmade Natural Products BM60	CIMICIFUGAD6, DROSERAD6, FORMICA RUFAD6, FULIGOD6, INULA HELD6, KALI MURD6, LAPIS ALBUSD6, SILICEAD6	Bestmade Natural Products	29912fb7-8712-18d9-e063-6394a90a82f7	2025-03-25	Warnings	Exact identifier unii: ETJ7Z6XBU4
it cosmetics Your Skin But Better CC Plus Oil Free Matte Poreless Finish Full Coverage Broad Spectrum SPF 40 Sunscreen All Shades	TITANIUM DIOXIDE AND ZINC OXIDE	IT COSMETICS, LLC	b7d184fb-4a9a-4720-9b00-bf0caa257a8c	2025-03-25	Warnings	Exact identifier unii: 15FIX9V2JP
Senna-S	SENNOSIDES AND DOCUSATE SODIUM	Meijer, Inc.	2619be6e-877b-16a2-e063-6394a90a68da	2025-03-24	Warnings	Exact identifier rxcui: 998740 unii: F05Q2T2JA0
Stool Softener plus Stimulant Laxative	DOCUSATE SODIUM AND SENNOSIDES	Meijer, Inc.	261a88d6-87d2-7544-e063-6294a90a2e94	2025-03-24	Warnings	Exact identifier rxcui: 998740 unii: F05Q2T2JA0
DOMINAS DARK SPOT TINTED SUNSCREEN	OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE	LG H&H CO., LTD.	2b6140cf-7e34-1658-e063-6394a90a3271	2025-03-24	Warnings	Exact identifier unii: 15FIX9V2JP
NAKED SUNDAYS CABANA GLOW MINERAL GLOW SERUM DROPS Illuminating 40mL with Pink Algae SPF 50	TITANIUM OXIDE, ZINC OXIDE	NAKED SUNDAYS PTY LTD	01273e8c-aef0-d800-e063-6294a90abd49	2025-03-23	Warnings	Exact identifier unii: 15FIX9V2JP
NAKED SUNDAYS CABANA GLOW MINERAL GLOW SERUM DROPS BRONZE 40mL with wild Rosella SPF 50	TITANIUM OXIDE, ZINC OXIDE	NAKED SUNDAYS PTY LTD	01221d57-9eec-7e77-e063-6394a90a6042	2025-03-23	Warnings	Exact identifier unii: 15FIX9V2JP
NAKED SUNDAYS CABANA GLOW MINERAL GLOW SERUM DROPS Blush 40mL SPF 50	TITANIUM OXIDE, ZINC OXIDE	NAKED SUNDAYS PTY LTD	0ce809a1-45fb-9d4d-e063-6294a90a26a2	2025-03-23	Warnings	Exact identifier unii: 15FIX9V2JP
Epsom Salt	MAGNESIUM SULFATE	CVS PHARMACY	30ce5cbd-cc7a-0b2d-e063-6394a90a8520	2025-03-20	Warnings	Exact identifier application number: M007
Senna	SENNOSIDES	AARNA USA INC.	7ad21fb7-20eb-48d6-be15-450aa2ec97d3	2025-03-20	Warnings	Exact identifier application number: M007

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.