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Soldanizer dn-723 - Medication Information

Product NDC Code 77015-100
Drug Name

Soldanizer dn-723

Type Brand
Active Ingredients
Benzalkonium chloride .13 g/100ml
Route TOPICAL
Dosage Form SPRAY
RxCUI drug identifier 1039012
Application Number part333A
Labeler Name 3VETS LLC
Packages
Package NDC Code Description
77015-100-04 118 ml in 1 bottle (77015-100-04)
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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 SPRAY PRODUCT INTO THE PALM OF HAND. RUB HANDS TOGETHER THOROUGHLY UNTIL DRY. SUPERVISE CHILDREN UNDER 6 YEARS OF AGE WHEN USING PRODUCT.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
INACTIVE INGREDIENTS WATER, DIDECYL DIMETHYL AMMONIUM CHLORIDE, PROPYLENE GLYCOL, METHYLPARABEN, DIAZOLIDINYL UREA, PROPYLPARABEN, COCAMIDOPROPYLAMINE OXIDE, ALLANTOIN, COCAMIDOPROPYL BETAINE, CETRIMONIUM CHLORIDE, TRIETHANOLAMINE, CITRIC ACID.

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 HAND SANITIZER HELPS REDUCE BACTERIA ON THE SKIN. CAN BE USED REPEATEDLY.

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.
SOLDANIZER DN-723 BENZALKONIUM CHLORIDE WATER DIDECYLDIMONIUM CHLORIDE PROPYLENE GLYCOL METHYLPARABEN DIAZOLIDINYL UREA PROPYLPARABEN COCAMIDOPROPYLAMINE OXIDE ALLANTOIN COCAMIDOPROPYL BETAINE CETRIMONIUM CHLORIDE TROLAMINE ANHYDROUS CITRIC ACID BENZALKONIUM CHLORIDE BENZALKONIUM

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.
LABEL

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. AVOID CONTACT WITH OR NEAR EYES WHEN USING THIS PRODUCT. IN CASE OF CONTACT, RINSE EYES THOROUGHLY WITH WATER. IF IRRITATION OR RASH APPEARS, OR IF CONDITION PERSISTS, STOP USE AND CONTACT A DOCTOR.

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