FDA.reportPublic FDA data

Foam - X

Manufacturer
Ideal Supplies, LLC
Effective date
2022-10-25
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:51:11

Label at a glance#

ProductFoam - X
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACTIVE Ingredients active ingredientactive ingredient

DOSAGE FORMS & STRENGTHS SECTION

dosagedosage

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

OTC- Keep out of reach ChildrenOTC- Keep out of reach Children

DOSAGE & ADMINISTRATION SECTION

Dosage DosageDosage

INACTIVE INGREDIENT SECTION

Inactive InactiveInactive

WARNINGS SECTION

Warninng WarningWarning

INDICATIONS & USAGE SECTION

Indication & Usage Indication & UsageIndication & Usage

OTC - PURPOSE SECTION

Purpose Section OTC-Purpose SectionOTC-Purpose Section

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabelLabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74407-011-012023-07-28C16284748780-1d6a99b39-5472-a426-e053-dadaa90af4c2a332c970-1ce7-6fd9-e053-2995a90a9252
74407-011-012022-02-16C16284748780-1d6a99b39-5472-a426-e053-dadaa90af4c2a332c970-1ce7-6fd9-e053-2995a90a9252
74407-011-012022-01-28C16284748780-1d6a99b39-5472-a426-e053-dadaa90af4c2a332c970-1ce7-6fd9-e053-2995a90a9252

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74407-011-01Foam - X473 mL in 1 BOTTLE, PUMPLIQUID4733

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74407-011FOAM - X (BENZALKONIUM CHLORIDE 0.13%) LIQUID [IDEAL SUPPLIES, LLC]3Legacy NDC, 1 package rows20221027_a332c970-1ce7-6fd9-e053-2995a90a9252.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74407-01174407-011-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
DIHYDROXYETHYL COCAMINE OXIDE8AR51R3BL5IACT
WATER059QF0KO0RIACT
GLYCERETH-17 COCOATE3057VPT0KCIACT
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
LAURTRIMONIUM CHLORIDEA81MSI0FICIACT
CETRIMONIUM CHLORIDEUC9PE95IBPIACT

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
ebde0719-498d-5889-e053-2a95a90acc6aa332c970-1ce7-6fd9-e053-2995a90a92522022-10-25WarningsExact identifier
spl id: ebde0719-498d-5889-e053-2a95a90acc6a
spl set id: a332c970-1ce7-6fd9-e053-2995a90a9252

Reported adverse events (FAERS/openFDA)#

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