FDA.reportPublic FDA data

White Rain Antibacterial Hand Spring Water

Manufacturer
International Wholesale, Inc.
Effective date
2025-05-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:02:18

Label at a glance#

ProductWhite Rain Antibacterial Hand Spring Water
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Indications and uses

for hand washing, reduces germs on the skin

Dosage and administration

Wash Hands and rinse.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

for hand washing, reduces germs on the skin

Warnings

WARNINGS SECTION

for external use only-hands only

Do Not use

OTC - DO NOT USE SECTION

on damaged or broken skin.

When using the product

OTC - WHEN USING SECTION

keep out of eyes. Rinse with water to remove.

Stop and consult a doctor if

OTC - STOP USE SECTION

irritation and redness develops.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions:

DOSAGE & ADMINISTRATION SECTION

Wash Hands and rinse.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Cetrimonium Chloride, Glycerin, Lauramidopropylamine Oxide and Myristamidopropylamine Oxide, Sodium Chloride, Cocamide MEA, PEG-120 Methyl Glucose Dioleate, Citric Acid, Fragance, Disodium EDTA, Methylchloroisothiazolinone, Methylisothiazolinone, Red 33, Blue 1

Other Information

SPL UNCLASSIFIED SECTION

Avoid Storing at extreme temperatures

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

bottkebottke

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapPSN1
1046593benzalkonium chloride 1.3 MG/ML Medicated Liquid SoapSCD1
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapSY1
1046593benzalkonium chloride 1.33 MG/ML Medicated Liquid SoapSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52862-626-00White Rain Antibacterial Hand Spring Water221 mL in 1 BOTTLE, PUMPSOAP2211

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
52862-62652862-626-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
EDETATE DISODIUM7FLD91C86KIACT
WATER059QF0KO0RIACT
CETRIMONIUM CHLORIDEUC9PE95IBPIACT
GLYCERINPDC6A3C0OXIACT
LAURAMIDOPROPYLAMINE OXIDEI6KX160QTVIACT
MYRISTAMIDOPROPYLAMINE OXIDE3HSF539C9TIACT
SODIUM CHLORIDE451W47IQ8XIACT
COCO MONOETHANOLAMIDEC80684146DIACT
PEG-120 METHYL GLUCOSE DIOLEATEYM0K64F20VIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
D&C RED NO. 339DBA0SBB0LIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

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
3634097e-f746-a9e1-e063-6294a90a779c960b3bc8-dffb-4eda-a71f-35754352e9b12025-05-28WarningsExact identifier
spl id: 3634097e-f746-a9e1-e063-6294a90a779c
spl set id: 960b3bc8-dffb-4eda-a71f-35754352e9b1

Reported adverse events (FAERS/openFDA)#

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