Softsoap Antibacterial with Moisturizers White Tea and Berry LHS

Manufacturer
Colgate-Palmolive Company | VeePak, Inc
Effective date
2024-10-29
Label type
HUMAN OTC DRUG LABEL
Version
9
Source
full-release
Hydrated at
2026-06-01 00:42:05

Label at a glance#

ProductSoftsoap Antibacterial with Moisturizers White Tea and Berry LHS
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Dosage and administration

wash hands and rinse

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Use

INDICATIONS & USAGE SECTION

helps eliminate bacteria on hands

Warnings

WARNINGS SECTION

For external use only.

OTC - WHEN USING SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children, except under adult supervision. 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, Cocamide MEA, Citric Acid, Sodium Benzoate, Fragrance, PEG-120 Methyl Glucose Dioleate, Sodium Chloride, Tetrasodium EDTA, Red 33, Blue 1.

Questions?

OTC - QUESTIONS SECTION

1-800-255-7552

SPL UNCLASSIFIED SECTION

DIST. BY:
COLGATE-PALMOLIVE COMPANY, NEW YORK, NY 10022 USA

PRINCIPAL DISPLAY PANEL - 332 mL Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Softsoap®

ANTIBACTERIAL
+
ELIMINATES 99.9%
OF BACTERIA*

ENRICHED WITH
MOISTURIZERS

white tea
& berry
scent

ANTIBACTERIAL HAND SOAP

11.25 FL OZ (332 mL)

PS0064350

PRINCIPAL DISPLAY PANEL - 332 mL Bottle Label
PRINCIPAL DISPLAY PANEL - 332 mL Bottle Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapPSN9
1367082Softsoap Antibacterial 0.13 % Medicated Liquid SoapPSN9
1367082benzalkonium chloride 1.3 MG/ML Medicated Liquid Soap [Softsoap Antibacterial]SBD9
1046593benzalkonium chloride 1.3 MG/ML Medicated Liquid SoapSCD9
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapSY9
1046593benzalkonium chloride 1.33 MG/ML Medicated Liquid SoapSY9
1367082Softsoap Antibacterial 0.13 % Medicated Liquid SoapSY9
1367082Softsoap Antibacterial 1.3 MG/ML Medicated Liquid SoapSY9

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
35000-101-11Softsoap Antibacterial with Moisturizers White Tea and Berry LHS332 mL in 1 BOTTLELIQUID3329

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
35000-101SOFTSOAP ANTIBACTERIAL WITH MOISTURIZERS WHITE TEA AND BERRY LHS (BENZALKONIUM CHLORIDE LIQUID) LIQUID [COLGATE-PALMOLIVE COMPANY]9Legacy NDC, 1 package rows20241212_a00d538e-c409-4dd6-aeb9-092d4ebab196.zip

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
35000-10135000-101-11

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

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
e82c117b-e539-47b5-817c-46fd22d3b4cba00d538e-c409-4dd6-aeb9-092d4ebab1962026-09-08WarningsExact identifier
spl set id: a00d538e-c409-4dd6-aeb9-092d4ebab196

Reported adverse events (FAERS/openFDA)#

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