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Coconut foaming hand sanitizer with natural vitamin e and almond oil - Medication Information

Product NDC Code 57660-004
Drug Name

Coconut foaming hand sanitizer with natural vitamin e and almond oil

Type Brand
Active Ingredients
Benzalkonium chloride 1.2 mg/ml
Route TOPICAL
Dosage Form LIQUID
RxCUI drug identifier 1046310
Application Number 505G(a)(3)
Labeler Name TJA Health LLC
Packages
Package NDC Code Description
57660-004-01 50 ml in 1 bottle, pump (57660-004-01)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
ACTIVE INGREDIENT Benzalkonium Chloride 0.12% PURPOSE Antimicrobial

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 Apply to dry hands, rub together, & let dry.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
INACTIVE INGREDIENTS Purified water, surfactant, vitamin E(natural, d-alpha tocopherol), almond oil (natural), polysorbate 20, isopropyl alcohol USP, natural essential oil complex, natutal coconut scent.

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.
USES For hand sanitizing to decrease bacteria on the skin Recommended for repeated use

Purpose

Information about the drug product’s indications for use.
PURPOSE Antimicrobial

Spl product data elements

Usually a list of ingredients in a drug product.
Coconut Foaming Hand Sanitizer With Natural Vitamin E and Almond Oil BENZALKONIUM CHLORIDE WATER .ALPHA.-TOCOPHEROL ALMOND OIL POLYSORBATE 20 BENZALKONIUM CHLORIDE BENZALKONIUM DIHYDROXYETHYL COCAMINE OXIDE ACETAMIDOETHOXYETHANOL COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE

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 Labeling: label

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

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 2 years of age and younger. If swallowed, get 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. Avoid contact with eyes. In case of eye contact, flush with water. Discontinue use if irritation or redness occurs. Keep out of reach of children 2 years of age and younger. If swallowed, get 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