FDA.reportPublic FDA data

NDC 68025-047-01 - Lorzone

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
68025-047
Requested NDC
68025-047-01
Package NDCs from labels
68025-047-10, 68025-047-01, 68025-047-02
Manufacturer
Vertical Pharmaceuticals, Inc.
Effective date
2023-09-29
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
LorzoneVertical Pharmaceuticals, Inc.2023-09-29HUMAN PRESCRIPTION DRUG LABEL

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
68025-047-10EA - Each68025-0477d8728a7-8b74-4dcd-b339-4d2b5abfe61f12012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
CHLORZOXAZONEACTIVE INGREDIENTH0DE420U8GLORZONE (CHLORZOXAZONE) TABLET [VERTICAL PHARMACEUTICALS, LLC]2
CHLORZOXAZONEACTIVE MOIETYH0DE420U8GLORZONE (CHLORZOXAZONE) TABLET [VERTICAL PHARMACEUTICALS, LLC]2
ANHYDROUS LACTOSEINACTIVE INGREDIENT3SY5LH9PMKLORZONE (CHLORZOXAZONE) TABLET [VERTICAL PHARMACEUTICALS, LLC]2
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61ULORZONE (CHLORZOXAZONE) TABLET [VERTICAL PHARMACEUTICALS, LLC]2
CROSCARMELLOSE SODIUMINACTIVE INGREDIENTM28OL1HH48LORZONE (CHLORZOXAZONE) TABLET [VERTICAL PHARMACEUTICALS, LLC]2
DOCUSATE SODIUMINACTIVE INGREDIENTF05Q2T2JA0LORZONE (CHLORZOXAZONE) TABLET [VERTICAL PHARMACEUTICALS, LLC]2
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30LORZONE (CHLORZOXAZONE) TABLET [VERTICAL PHARMACEUTICALS, LLC]2
SODIUM BENZOATEINACTIVE INGREDIENTOJ245FE5EULORZONE (CHLORZOXAZONE) TABLET [VERTICAL PHARMACEUTICALS, LLC]2
STARCH, CORNINACTIVE INGREDIENTO8232NY3SJLORZONE (CHLORZOXAZONE) TABLET [VERTICAL PHARMACEUTICALS, LLC]2

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 6 of 19 · 373 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Stool Softener Laxative Extra StrengthDOCUSATE SODIUMP & L Development, LLC33000a06-e030-433a-8f9c-7ae5c08037fa2026-01-06WarningsExact identifier
unii: F05Q2T2JA0
Stool Softener Regular StrengthDOCUSATE SODIUMSam's West, Inc1eca5910-b0bf-4e07-8211-36dba52b3de72026-01-06WarningsExact identifier
unii: F05Q2T2JA0
Senna SDOCUSATE SODIUM, SENNOSIDESSafeway, Inc.acb40b29-5fd5-4864-b6bf-4102e47a16832026-01-05WarningsExact identifier
unii: F05Q2T2JA0
Senna-SSENNOSIDES AND DOCUSATE SODIUMRMT HEALTH LLC4742182e-fdf9-44fe-e063-6394a90adfcc2025-12-31WarningsExact identifier
unii: F05Q2T2JA0
Docusate Sodium LiquidDOCUSATE SODIUMLLORENS PHARMACEUTICALS INTERNATIONAL DIVISION2d8bdd3e-f6e6-43f5-b3b0-e5a882cae41c2025-12-31WarningsExact identifier
unii: F05Q2T2JA0
Senna-SDOCUSATE SODIUM 50MG AND SENNOSIDES 8.6MGWalgreens36cc3a5b-1891-d39e-e063-6294a90a93b42025-12-31WarningsExact identifier
unii: F05Q2T2JA0
Docusate Sodium LiquidDOCUSATE SODIUMRUGBY LABORATORIESe21d19d8-6c2d-4474-a663-dfe7e91ac3202025-12-30WarningsExact identifier
unii: F05Q2T2JA0
Senna-SSENNA-SPioneer Life Sciences, LLCab46a3ca-6c7a-a81e-e053-2995a90a199f2025-12-29WarningsExact identifier
unii: F05Q2T2JA0
Medicated Cornstarch Baby PowderACTIVE CORN STARCHDavion, Inc.e39032d1-c8cd-4a41-af10-126970b8ad382025-12-29WarningsExact identifier
unii: O8232NY3SJ
Senna-SSENNOSIDES 8.6MG AND DOCUSATE SODIUM 50MGPharbest Pharmaceuticals, Inc.2b5152b2-d354-409f-a19f-b470f4181b3f2025-12-24WarningsExact identifier
unii: F05Q2T2JA0
Senna PlusDOCUSATE SODIUM 50 MG AND SENNOSIDES 8.6 MGCARDINAL HEALTH, 110 DBA LEADER4d4101ca-7d78-4712-9b3d-f395f2646c6b2025-12-23WarningsExact identifier
unii: F05Q2T2JA0
Senna-SSENNOSIDES 8.6 MG AND DOCUSATE SODIUM 50 MGNUVICARE LLC9e999e4a-2f72-4a2b-a41b-bdd68bf5a3502025-12-19WarningsExact identifier
unii: F05Q2T2JA0
Stool Softener LaxativeDOCUSATE SODIUMP & L Development, LLCcb0765cb-f48e-4daa-97b8-2897a2d955872025-12-19WarningsExact identifier
unii: F05Q2T2JA0
Stool Softener LaxativeDOCUSATE SODIUMStrategic Sourcing Services LLCba51cca1-b70b-476e-80e6-20cd52292e652025-12-17WarningsExact identifier
unii: F05Q2T2JA0
Stool Softener Extra StrengthDOCUSATE SODIUMCVS Pharmacya694b4f3-6112-4a1d-a06e-9e5b20fd3d7b2025-12-17WarningsExact identifier
unii: F05Q2T2JA0
Stool Softener LaxativeDOCUSATE SODIUMCARDINAL HEALTH 110, LLC. DBA LEADER 70000da5ccd75-8a2f-4f90-ae8a-97d81b8579d22025-12-17WarningsExact identifier
unii: F05Q2T2JA0
Senna PlusDOCUSATE SODIUM, SENNOSIDESCVS Pharmacyae9d1672-9ade-4139-9126-5289b87fe5742025-12-17WarningsExact identifier
unii: F05Q2T2JA0
GeriCare Docusate Sodium LiquidDOCUSATE SODIUMGERI-CARE PHARMACEUTICALS, CORPd599ff49-c9a4-401a-a50b-63d89749bbed2025-12-11WarningsExact identifier
unii: F05Q2T2JA0
Docusate SodiumDOCUSATE SODIUMMajor Pharmaceuticals3e8321cf-7eda-d70c-e063-6394a90a35a52025-12-10WarningsExact identifier
unii: F05Q2T2JA0
Stool SoftenerDOCUSATE SODIUMHEB2f103a88-4cab-d4b9-e063-6394a90ac7fc2025-12-09WarningsExact identifier
unii: F05Q2T2JA0

Reported adverse events (FAERS/openFDA)#

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