FDA.reportPublic FDA data

LACTIC ACID 10% / UREA 40%

Manufacturer
Sincerus Florida, LLC
Effective date
2019-05-17
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 20:28:49

Label at a glance#

ProductLACTIC ACID 10% / UREA 40%
Active ingredientUREA, LACTIC ACID
Label structure4 sections

Label contents#

Full prescribing information#

Directions for use

INSTRUCTIONS FOR USE SECTION

sdsd

Sincerus Flordia, LLC. Adverse reactions

ADVERSE REACTIONS SECTION

dada

Active, Inactive

COMPONENTS

asdasd

NDC 72934- 1135-4 LACTIC ACID 10% / UREA 40% . Gel 120gm

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

zczc

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
LACTIC ACID, UNSPECIFIED FORM Pharmacologic Class Indexing1Indexing - Pharmacologic Class20220121

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
597b1cfd-7b31-5048-62be-ca5cd740da2fProduct name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72934-1135-42021-01-29C16284748780-1ba0f9c33-26fe-a910-e053-dadaa90a0b85LACTIC ACID 10% / UREA 40%

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72934-1135-4LACTIC ACID 10% / UREA 40%120 g in 1 BOTTLE, PUMPGEL1201

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72934-1135LACTIC ACID 10% / UREA 40% GEL [SINCERUS FLORIDA, LLC]1Legacy NDC, 1 package rows20190518_89194cae-d42c-7ab5-e053-2a95a90ad805.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72934-113572934-1135-4

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
UREA8W8T17847WACTIB
LACTIC ACID33X04XA5ATACTIB

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
89194cae-d42d-7ab5-e053-2a95a90ad80589194cae-d42c-7ab5-e053-2a95a90ad8052019-05-17Adverse reactionsExact identifier
spl id: 89194cae-d42d-7ab5-e053-2a95a90ad805
spl set id: 89194cae-d42c-7ab5-e053-2a95a90ad805

Reported adverse events (FAERS/openFDA)#

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