FDA.reportPublic FDA data

Pop Ocean Antibacterial

Manufacturer
MINGSHI TECHNOLOGY CO., LTD
Effective date
2021-12-02
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:25:04

Label at a glance#

ProductPop Ocean Antibacterial
Active ingredientBENZALKONIUM CHLORIDE
Label structure11 sections

Indications and uses

For hand washing to decrease bacteria on the skin

Dosage and administration

For personal domestic use. Lather in hands with water for at least 30 seconds. Rinse well Supervise children when using this product.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

For hand washing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For External Use only.

When using this product

OTC - WHEN USING SECTION

do not get into eyes. If contact occurs, rinse eyes thoroughly with water

Stop use

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation and redness develop 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 right away

Directions

DOSAGE & ADMINISTRATION SECTION

For personal domestic use. Lather in hands with water for at least 30 seconds. Rinse well

Supervise children when using this product.

Other Information

OTHER SAFETY INFORMATION

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

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Sodium Laureth Sulfate,Glycerin, Lauryl Glucoside, Cocoamidopropyl Betaine, Cocamide Methyl Mea, Phenoxyethanol, Aloe Barbadensis Leaf Extract, Sodium Chloride, Fragrance, Glycol Distearate, Ethylhexylglicerin, Benzophenone-4, Laureth-4, Citric Acid, Sodium Hydroxide, Blue 1 (CI 42090) Yellow 5 (CI 19140)

Pop arazzi Ocean Antibacterial Liquid Hand Soap

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73992-003-672021-12-02C16284748780-1c7ccaba7-10ec-fd44-e053-dadaa90aa01bPop•arazzi Ocean Antibacterial Liquid Hand Soap
73992-003-672021-07-23C16284748780-1c7ccaba7-10ec-fd44-e053-dadaa90aa01bPop•arazzi Ocean Antibacterial Liquid Hand Soap

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73992-00373992-003-67

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
SODIUM HYDROXIDE55X04QC32IIACT
SULISOBENZONE1W6L629B4KIACT
COCAMIDE3YXD33R71GIACT
LAURETH-46HQ855798JIACT
SODIUM LAURETH SULFATEBPV390UAP0IACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
LAURYL GLUCOSIDE76LN7P7UCUIACT
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
PHENOXYETHANOLHIE492ZZ3TIACT
SODIUM CHLORIDE451W47IQ8XIACT
GLYCOL DISTEARATE13W7MDN21WIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
ALOE VERA LEAFZY81Z83H0XIACT

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
eff4402b-6564-a51d-e053-2995a90a48a8aed89570-414f-ffe0-e053-2a95a90aef672022-12-16WarningsExact identifier
spl set id: aed89570-414f-ffe0-e053-2a95a90aef67

Reported adverse events (FAERS/openFDA)#

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