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Escudo ultra-protect original - Medication Information

Product NDC Code 84529-001
Drug Name

Escudo ultra-protect original

Type Brand
Active Ingredients
Benzalkonium chloride .1 g/100g
Route TOPICAL
Dosage Form SOAP
RxCUI drug identifier 1926450
Application Number M003
Labeler Name Indelpa, Inc
Packages
Package NDC Code Description
84529-001-01 115 g in 1 cello pack (84529-001-01)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredient Active Ingredient ------------------------------- Purpose Benzalkonium Chloride 0.1% ----------------- Antibacterial Active Ingredient ------------------------------- Purpose Benzalkonium Chloride 0.1% ----------------- Antibacterial

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 Wet bar with water. Lather vigorously and wash skin. Rinse with water and dry thoroughly.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredients Alcohol, D&C Red 33, Etidronic Acid, FD&C Green 3, Glycerin, Sodium Chloride, Sodium Palmate, Sodium Palm Kernelate, Tetrasodium EDTA, Titanium Dioxide, Water, Fragance.

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 washing to decrease becateria on the skin.

Purpose

Information about the drug product’s indications for use.
Active Ingredient ------------------------------- Purpose Benzalkonium Chloride 0.1% ----------------- Antibacterial

Spl product data elements

Usually a list of ingredients in a drug product.
Escudo Ultra-Protect Original Benzalkonium Chloride WATER ETIDRONIC ACID GLYCERIN BENZALKONIUM CHLORIDE BENZALKONIUM SODIUM CHLORIDE FD&C GREEN NO. 3 EDETATE SODIUM D&C RED NO. 33 FRAGRANCE 13576 SODIUM PALMATE TITANIUM DIOXIDE ALCOHOL SODIUM PALM KERNELATE Escudo;ULTRA;PROTECT

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.
Package Label principal display panel Eliminates 99.9% of Bacteria Fresh clean scent Deep cleansing Escudo® ULTRA-PROTECT ORIGINAL ANTIBACTERIAL BAR SOAP NET WT 4.05 Z (115g) Escudo Ultra-Protect Original

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 *effective only against E. coli and S. Aureus. Distributed by Indelpa, Inc. 18911 Hardy Oak Blvd Suite 327 San Antonio, TX 78258. MADE IN COLOMBIA

Do not use

Information about all contraindications for use. These contraindications are absolute and are intended for situations in which consumers should not use the product unless a prior diagnosis has been established by a doctor or for situations in which certain consumers should not use the product under any circumstances regardless of whether a doctor or health professional is consulted.
Do not use if you are allergic to any of the ingredients

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.

Questions

A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.
Questions or Comments? 1-800-678-5082 [email protected]

Stop use

Information about when use of the drug product should be discontinued immediately and a doctor consulted. Includes information about any signs of toxicity or other reactions that would necessitate immediately discontinuing use of the product.
Stop use and ask a doctor if irritation or redness develop and persist for more than 72 hours.

When using

Information about side effects that people may experience, and the substances (e.g. alcohol) or activities (e.g. operating machinery, driving a car) to avoid while using the drug product.
When using this product avoid contact with eyes. In case of eye contact, rinse thoroughly with water.

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. Do not use if you are allergic to any of the ingredients Directions Wet bar with water. Lather vigorously and wash skin. Rinse with water and dry thoroughly. When using this product avoid contact with eyes. In case of eye contact, rinse thoroughly with water. Stop use and ask a doctor if irritation or redness develop and persist for more than 72 hours. 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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