Pop•arazzi Ocean Antibacterial Liquid Hand Soap

Pop Ocean Antibacterial by

Drug Labeling and Warnings

Pop Ocean Antibacterial by is a Otc medication manufactured, distributed, or labeled by MINGSHI TECHNOLOGY CO., LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

POP OCEAN ANTIBACTERIAL- benzalkonium chloride 0.13% liquid 
MINGSHI TECHNOLOGY CO., LTD

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Poparazzi Ocean Antibacterial Liquid Hand Soap

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antiseptic

Uses

For hand washing to decrease bacteria on the skin

Warnings

For External Use only.

When using this product

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

Stop use

Stop use and ask a doctor if irritation and redness develop and lasts

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away

Directions

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

Supervise children when using this product.

Other Information

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

Inactive Ingredients

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

POP OCEAN ANTIBACTERIAL 
benzalkonium chloride 0.13% liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73992-003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.26 g  in 200 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM HYDROXIDE (UNII: 55X04QC32I)
SULISOBENZONE (UNII: 1W6L629B4K)
COCAMIDE (UNII: 3YXD33R71G)
LAURETH-4 (UNII: 6HQ855798J)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
GLYCOL DISTEARATE (UNII: 13W7MDN21W)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73992-003-67	200 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	08/01/2020	12/31/2022

Labeler - MINGSHI TECHNOLOGY CO., LTD (542992088)

Revised: 12/2022

Document Id: eff4402b-6564-a51d-e053-2995a90a48a8

34390-5

Set id: aed89570-414f-ffe0-e053-2a95a90aef67

Version: 3

Effective Time: 20221216