CaseysLavender

Manufacturer
KYNC Design LLC
Effective date
2026-01-23
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
full-release
Hydrated at
2026-06-01 01:35:06

Label at a glance#

ProductCaseysLavender
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Dosage and administration

Wash hands and rinse

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride (CAS NO: 68424-85-1), 0.13% .

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

Helps eliminate bacteria on hands

WARNINGS

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

If you are allergic to any of the ingredients.

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation or rash occurs.

Do not use in or near the eyes.

OTC - WHEN USING SECTION

In case of contact, rinse eyes thoroughly with water. Stop use and ask a doctor if irritation or rash appears and lasts.

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 immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Wash hands and rinse

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Anhydrous Citric Acid, Cocamidopropylamine Oxide, Edetate Sodium, Fragrance, Glycerin, Lauramine Oxide, Magnesium Chloride, Magnesium Nitrate, Methylchloroisothiazolinone, Methylisothiazolinone, PEG-120 Methyl Glucose Dioleate, PEG-4 Rapeseedamide, Styrene/acrylamide Copolymer (mw 500000), Colorant CI 60725, Lavandula Angustifola Extract.

OTC - PURPOSE SECTION

Antibacterial

PRODUCT LABELS

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Caseys1Caseys1

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapPSN7
1046593benzalkonium chloride 1.3 MG/ML Medicated Liquid SoapSCD7
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapSY7
1046593benzalkonium chloride 1.33 MG/ML Medicated Liquid SoapSY7

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130098437243824GTIN-13: 0098437243824
EAN-13: 0098437243824
GTIN-12: 098437243824
UPC-A: 098437243824
GTIN storage (14 digits): 00098437243824
Caseys Handsoap.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76557-051-01CaseysLavender500 g in 1 BOTTLE, PUMPLIQUID5007

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
76557-05176557-051-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 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
CaseysLavenderCASEYS HAND SOAP LAVENDER SCENTKYNC Design LLCb5bc8770-13ef-36dc-e053-2995a90a3f512026-01-23WarningsExact identifier
ndc (package): 76557-051-01
ndc (product): 76557-051
ndc11 (package): 76557005101
spl id: 49118bfc-70da-b9c4-e063-6394a90a0055
spl set id: b5bc8770-13ef-36dc-e053-2995a90a3f51

Reported adverse events (FAERS/openFDA)#

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