TACROLIMUS 0.1%

Manufacturer: Sincerus Florida, LLC
Effective date: 2019-05-09
Label type: HUMAN PRESCRIPTION DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 20:28:39

Label at a glance#

ProductTACROLIMUS 0.1%

Active ingredientTACROLIMUS

Label structure4 sections

Label contents#

Full prescribing information#

Directions for use

INSTRUCTIONS FOR USE SECTION

Sincerus Florida, LLC. Adverse reactions

ADVERSE REACTIONS SECTION

Active, inactive

COMPONENTS

NDC 72934-4173-8. TACROLIMUS MONOHYDRATE USP 0.1%. Solution 60 gm.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DailyMed Pharmacologic Classes#

Class, Version, Type table
Class	Version	Type	Effective
TACROLIMUS ANHYDROUS Pharmacologic Class Indexing	3	Indexing - Pharmacologic Class	20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
df369ad4-19d8-393a-de46-8c6255b8b360	Product name	8	20251120
d2a74186-7b26-dbcc-9435-50b3d0be14ab	Product name	2	20250114
a64835ae-fa9d-41d8-9a93-36828ba72b96	Product name	3	20190611
b4a869e4-9fcd-47bd-95e3-85e7c75f8bad	Product name	1	20150819

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
72934-4173-8	2021-01-29	C162847	48780-1	ba0f9c33-1242-a910-e053-dadaa90a0b85	TACROLIMUS 0.1%

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
72934-4173-8	TACROLIMUS 0.1%	60 g in 1 BOTTLE, GLASS	SOLUTION	60		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72934-4173	TACROLIMUS 0.1% SOLUTION [SINCERUS FLORIDA, LLC]	1	Legacy NDC, 1 package rows	20190510_8875fc25-e9f0-4221-e053-2995a90afc97.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 3 matching rows.

TACROLIMUS 0.1%
TACROLIMUS
TACROLIMUS ANHYDROUS

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
72934-4173	72934-4173-8

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 1 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
TACROLIMUS	WM0HAQ4WNM	ACTIM

Source Document#

Source XML

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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
8875fc25-e9f1-4221-e053-2995a90afc97			8875fc25-e9f0-4221-e053-2995a90afc97	2019-05-09	Adverse reactions	Exact identifier spl id: 8875fc25-e9f1-4221-e053-2995a90afc97 spl set id: 8875fc25-e9f0-4221-e053-2995a90afc97

Reported adverse events (FAERS/openFDA)#

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