FDA.reportPublic FDA data

Foamy Blue

Manufacturer
Pro Chem Solutions, Inc.
Effective date
2025-05-05
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:00:43

Label at a glance#

ProductFoamy Blue
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Dosage and administration

Apply a palmful to hands and forearms. Scrub thoroughly for at least fifteen seconds. Rinse completely and dry.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1%

Purpose

OTC - PURPOSE SECTION

Skin Antimicrobial

Use

INDICATIONS & USAGE SECTION

reduces amount of bacteria on hands

Warnings

WARNINGS SECTION

For external use only.

When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.

Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Apply a palmful to hands and forearms.
  • Scrub thoroughly for at least fifteen seconds.
  • Rinse completely and dry.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Lauramine Oxide, Glycerin, PEG-120 Methyl Glucose Dioleate, DMDM Hydantoin, Citric Acid, Fragrance, Blue 1

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package Label - 1000 mL BagPackage Label - 1000 mL Bag

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1233282benzalkonium chloride 0.1 % Medicated Liquid SoapPSN4
1233282benzalkonium chloride 1 MG/ML Medicated Liquid SoapSCD4
1233282benzalkonium chloride 0.1 % Medicated Liquid SoapSY4

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83188-405-04Foamy Blue1000 mL in 1 BAGSOLUTION10004

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83188-405FOAMY BLUE (BENZALKONIUM CHLORIDE) SOLUTION [PRO CHEM SOLUTIONS, INC.]4Current NDC, 1 package rows20250510_aafecb36-082a-4577-a06a-4a5460e21a1d.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
83188-40583188-405-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
PEG-120 METHYL GLUCOSE DIOLEATEYM0K64F20VIACT
LAURAMINE OXIDE4F6FC4MI8WIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
DMDM HYDANTOINBYR0546TOWIACT

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
Foamy BlueBENZALKONIUM CHLORIDEPro Chem Solutions, Inc.aafecb36-082a-4577-a06a-4a5460e21a1d2025-05-05WarningsExact identifier
ndc (package): 83188-405-04
ndc (product): 83188-405
ndc11 (package): 83188040504
spl id: 34681507-5fc9-496f-e063-6394a90a51b5
spl set id: aafecb36-082a-4577-a06a-4a5460e21a1d

Reported adverse events (FAERS/openFDA)#

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