FDA.reportPublic FDA data

The Spathecary Foaming Lavender

Manufacturer
Larry (Xiamen) Hi Tech Co., Ltd | G2 Beauty Inc
Effective date
2020-10-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:31:35

Label at a glance#

ProductThe Spathecary Foaming Lavender
Active ingredientBENZALKONIUM CHLORIDE
Label structure12 sections

Indications and uses

to help reduce bacteria that potentially can cause disease.

Dosage and administration

Pump into hands, wet as needed. Lather vigorously for at least 20 seconds. Wash skin, rinse thoroughly, and dry.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

to help reduce bacteria that potentially can cause disease.

Warnings

WARNINGS SECTION

For external use only.

When using this product

OTC - WHEN USING SECTION

When using this product. Avoid contact with eyes. In case of eye contact, rinse eyes thoroughly with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation or rash occurs. These may be signs of a serious condition.

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

Pump into hands, wet as needed. Lather vigorously for at least 20 seconds. Wash skin, rinse thoroughly, and dry.

Other Information

OTHER SAFETY INFORMATION

Store between 15-30C (59-86F)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

aqua/water/EAU, Sodium Laureth Sulfate, cocamidopropylamine oxide, cocamidopropyl betaine, glycerin, parfum, methylchloroisothiazolinone, Methylisothiazolinone, Magnesium chloride, Magnesium nitrate, Aloe Barbadensis Leaf Juice, Disodium EDTA, Citric Acid, Tocopheryl Acetate, FD &C yellow No.5 (CI 19140), FD&C Red No. 33 (CI 17200), FD&C Blue No. 1 (CI 42090)

Questions or Comments?

OTC - QUESTIONS SECTION

P.O. Box 230258, Brooklyn, NY 11223

The Spathecary Foaming Hand Soap Lavender

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73166-111-162022-01-28C16284748780-1d6a99b39-62ce-a426-e053-dadaa90af4c2The Spathecary Foaming Hand Soap Lavender

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73166-111-16The Spathecary Foaming Lavender500 mL in 1 BOTTLESOAP5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73166-111THE SPATHECARY FOAMING LAVENDER (BENZALKONIUM CHLORIDE 0.13%) SOAP [LARRY (XIAMEN) HI TECH CO., LTD]1Legacy NDC, 1 package rows20201014_b1916fbe-58f4-41ab-e053-2995a90a86f4.zip

Products#

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

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73166-11173166-111-16

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOE VERA LEAFZY81Z83H0XIACT
MAGNESIUM NITRATE77CBG3UN78IACT
MAGNESIUM CHLORIDE ANHYDROUS59XN63C8VMIACT
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
GLYCERINPDC6A3C0OXIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
SODIUM LAURETH SULFATEBPV390UAP0IACT
DISODIUM EDTA-COPPER6V475AX06UIACT
FD&C YELLOW NO. 5I753WB2F1MIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
D&C RED NO. 339DBA0SBB0LIACT
COCAMIDOPROPYLAMINE OXIDEM4SL82J7HKIACT

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
b1916fbe-58f5-41ab-e053-2995a90a86f4b1916fbe-58f4-41ab-e053-2995a90a86f42020-10-13WarningsExact identifier
spl id: b1916fbe-58f5-41ab-e053-2995a90a86f4
spl set id: b1916fbe-58f4-41ab-e053-2995a90a86f4

Reported adverse events (FAERS/openFDA)#

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