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Prevent - Medication Information

Product NDC Code 66077-708
Drug Name

Prevent

Type Brand
Active Ingredients
Chloroxylenol 3.75 mg/ml
Route TOPICAL
Dosage Form SOAP
RxCUI drug identifier 1362618
Application Number part333A
Labeler Name Ultra-Chem Inc.
Packages
Package NDC Code Description
66077-708-55 208 ml in 1 drum (66077-708-55)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Prevent ​Active Ingredient Chloroxylenol 0.375%

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.
Prevent Directions ​Read the entire label before using this product. ​Dispense 1-2 pumps of product onto wet palm. Lather and rinse hands with clean water

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Prevent Inactive Ingredients ​Water, Sodium Lauryl lSulfate, Cocamide DEA, Cocamidopropyl betadine, Phenoxyethanol, Sodium Laureth Sulfate, Propylene Glycol, Fragrance, DMDM Hydantoin, Glycol Stearate, Laurimide DEA, Glycerine, Tocopheryl Acetate, D&C Green #5, FD&C Yellow #5.

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.
Prevent Uses ​ ​Antibacterial hand cleaner. Use in daycare, hospitals, nursing homes, physicians offices, dental offices and clinics

Purpose

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

Spl product data elements

Usually a list of ingredients in a drug product.
Prevent Chloroxylenol BENZYL BENZOATE SODIUM HYDROXIDE METHYL ANTHRANILATE SODIUM ALUMINIUM SILICATE ETHYL ACETOACETATE GLYCOL DISTEARATE .GAMMA.-DECALACTONE ETHYLENE OXIDE WATER SODIUM LAURYL SULFATE COCO DIETHANOLAMIDE COCAMIDOPROPYL BETAINE PHENOXYETHANOL PROPYLENE GLYCOL ETHYL BUTYRATE LAURIC DIETHANOLAMIDE CALCIUM SILICATE CALCIUM CATION D&C GREEN NO. 5 FD&C YELLOW NO. 5 CHLOROXYLENOL CHLOROXYLENOL DIOXANE DIMETHYL BENZYL CARBINYL ACETATE METHYLISOTHIAZOLINONE MAGNESIUM NITRATE SODIUM CARBONATE METHYLCHLOROISOTHIAZOLINONE TRIBASIC CALCIUM PHOSPHATE SODIUM FERROCYANIDE LAURIC ISOPROPANOLAMIDE METHYL ALCOHOL ETHYL METHYLPHENYLGLYCIDATE LINALOOL, (+/-)- CHLOROACETIC ACID DIMETHYL BENZYL CARBINYL BUTYRATE

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.
Prevent UltraChem 141 UltraChem 141

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.
Prevent Winning Hands Antibacterial KEEP OUT OF REACH OF CHILDREN

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.
Prevent Warnings For external use only. Avoid contact with eyes. Children under the age of 6 should be supervised by an adult when using this product. Discontinue use is irritation or redness develops. If irritation persists for more than 72 hours, consult a physician. KEEP OUT OF REACH OF CHILDREN .

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