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Breeze antibacterial handsoap lavender and jasmine - Medication Information

Product NDC Code 74955-031
Drug Name

Breeze antibacterial handsoap lavender and jasmine

Type Brand
Active Ingredients
Benzalkonium chloride .13 g/100ml
Route TOPICAL
Dosage Form LIQUID
RxCUI drug identifier 1046593
Application Number part333E
Labeler Name COSMOLIVE KOZMETIK SANAYI VE TICARET ANONIM SIRKETI
Packages
Package NDC Code Description
74955-031-01 500 ml in 1 bottle, pump (74955-031-01)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredient Benzalkonium Chloride 0.13%

Dosage and administration

Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.
Directions • Pump into hands, wet as needed • Lather vigorously for at least 15 seconds • Wash skin, rinse thoroughly and dry

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients Aqua, Benzophenone-4, Citric Acid, Cocamide DEA, Cocamidopropyl Betaine, DMDM Hydantoin, FD&C Blue No:1, FD&C Red No. 40, Glycerin, Methylchloroisothiazolinone, Methylisothiazolinone, Parfum, Sodium Chloride, Sodium Laureth Sulfate, Tetrasodium EDTA.

Indications and usage

A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.
Use • For handwashing to decrease bacteria on the skin

Purpose

Information about the drug product’s indications for use.
Purpose Antibacterial

Spl product data elements

Usually a list of ingredients in a drug product.
BREEZE ANTIBACTERIAL HANDSOAP LAVENDER AND JASMINE Benzalkonium chloride BENZALKONIUM CHLORIDE BENZALKONIUM WATER SULISOBENZONE CITRIC ACID MONOHYDRATE COCO DIETHANOLAMIDE COCAMIDOPROPYL BETAINE DMDM HYDANTOIN FD&C BLUE NO. 1 FD&C RED NO. 40 GLYCERIN METHYLCHLOROISOTHIAZOLINONE METHYLISOTHIAZOLINONE SODIUM CHLORIDE SODIUM LAURETH-3 SULFATE EDETATE SODIUM

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
Packaging IMAGE

Spl unclassified section

Information not classified as belonging to one of the other fields. Approximately 40% of labeling with effective_time between June 2009 and August 2014 have information in this field.
Drug Facts Extra Soft CLEANSING MOISTURIZING REFRESHING UNAC GROUP KOZMETİK SAN. TİC. LTD. ŞTİ Trump Towers Residence No: 12/238 D.No:606 Şişli, Istanbul- TURKEY - Tel: +90 212 526 68 69 www.unac.com.tr USA DISTRIBUTOR: UNAC INTERNATIONAL INC. / [email protected] Made in TURKEY

Keep out of reach of children

Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Warnings

Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.
Warnings For external use only When using this product • Avoid contact with eyes. In case of eye contact, rinse eyes thoroughly with water. Stop use and ask a doctor if irritation and redness develops. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API

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