FDA.reportPublic FDA data

NDC-41226-510, Kroger Moisturizing spring water antibacterial Hand Soap

Manufacturer
Kroger Company | Apollo Health and Beauty Care
Effective date
2026-05-04
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 01:56:06

Label at a glance#

ProductKroger Springwater Antibacterial
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Indications and uses

Helps decrease bacteria on hands.

Dosage and administration

From pump bottle, apply onto wet hands. Lather and rinse thoroughly.

Storage and handling

Store at room temperature.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

Helps decrease bacteria on hands.

Warnings

WARNINGS SECTION

For external use only.

When using the product

OTC - WHEN USING SECTION

Avoid contact with eyes. In case of Contact, Flush with Water.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, seek medical attention or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • From pump bottle, apply onto wet hands.
  • Lather and rinse thoroughly.

Other Information

STORAGE AND HANDLING SECTION

Store at room temperature.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Lauramidopropylamine Oxide, Glycerin, Cetrimonium Chloride, Sodium Chloride, Cocamide MEA, PEG-120 Methyl Glucose Dioleate, Fragrance (Parfum), Citric Acid, Tetrasodium EDTA, Sodium Sulfate, Methylchloroisothiazolinone, Methylisothiazolinone, Blue 1 (CI42090), Red 33 (CI 17200).

PDP-1, NDC- 41226-510-11

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1111

PDP-2, NDC- 41226-510-52

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

5252

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapPSN5
1046593benzalkonium chloride 1.3 MG/ML Medicated Liquid SoapSCD5
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapSY5
1046593benzalkonium chloride 1.33 MG/ML Medicated Liquid SoapSY5

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130041260025273GTIN-13: 0041260025273
EAN-13: 0041260025273
GTIN-12: 041260025273
UPC-A: 041260025273
GTIN storage (14 digits): 00041260025273		06-26730-31.jpg
BarcodeEAN-130041260025280GTIN-13: 0041260025280
EAN-13: 0041260025280
GTIN-12: 041260025280
UPC-A: 041260025280
GTIN storage (14 digits): 00041260025280		06-26732-33.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
f1e0dc7e-7d61-4625-b6d9-4894927679d7Product name220211025
3c386306-c48a-413e-bb69-70cb268496f3Product name120210727
e4870509-7e28-6f92-f0be-dd3dd889a9cfProduct name520200810
6e9d4a47-c464-b93e-aebc-ad7bffc9c4cdProduct name220190619
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
5668b646-cd56-c3c7-bdea-3f6b1a8840dbProduct name120140508
684ea482-2e8b-14af-5664-b98f1e402036Product name120140508
810ab97e-f109-f41c-7c83-6a652a9cbf43Product name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct name120140508
b060cc1a-fe47-856b-0b77-4448b5963de8Product name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
41226-510-11Kroger Springwater Antibacterial325 mL in 1 BOTTLE, PLASTICLIQUID3255
41226-510-52Kroger Springwater Antibacterial1540 mL in 1 BOTTLE, PLASTICLIQUID15405

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
41226-51041226-510-11, 41226-510-52

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
EDETATE SODIUMMP1J8420LUIACT
FRAGRANCE CLEAN ORC0600327329LCV5BTFIACT
GLYCERINPDC6A3C0OXIACT
CETRIMONIUM CHLORIDEUC9PE95IBPIACT
SODIUM CHLORIDE451W47IQ8XIACT
LAURAMIDOPROPYLAMINE OXIDEI6KX160QTVIACT
COCO MONOETHANOLAMIDEC80684146DIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
PEG-120 METHYL GLUCOSE DIOLEATEYM0K64F20VIACT
SODIUM SULFATE0YPR65R21JIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
D&C RED NO. 339DBA0SBB0LIACT
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
Kroger Springwater AntibacterialBENZALKONIUM CHLORIDEKroger Company01006967-d11c-d02a-e063-6394a90ad42c2026-05-04WarningsExact identifier
ndc (package): 41226-510-11
ndc (package): 41226-510-52
ndc (product): 41226-510
ndc11 (package): 41226051011
ndc11 (package): 41226051052
spl id: 51025c60-925f-6971-e063-6394a90ae0a6
spl set id: 01006967-d11c-d02a-e063-6394a90ad42c

Reported adverse events (FAERS/openFDA)#

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