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Skinsei - Medication Information

Product NDC Code 64942-1740
Drug Name


Type Brand
Active Ingredients
Alcohol 700 mg/ml
Dosage Form LIQUID
RxCUI drug identifier 582753
Application Number part333E
Labeler Name Conopco Inc. d/b/a/ Unilever
Package NDC Code Description
64942-1740-1 118 ml in 1 container (64942-1740-1)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Drug Facts Active ingredient Ethyl Alcohol 70%


General information about the drug product, including the proprietary and established name of the drug, the type of dosage form and route of administration to which the label applies, qualitative and quantitative ingredient information, the pharmacologic or therapeutic class of the drug, and the chemical name and structural formula of the drug.
SKINSEI HAND SANITIZER - Alcohol liquid Skinsei Hand Sanitizer

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 • Place enough product in your palm to thoroughly spread on both hands and rub into the skin until dry. Recommended for repeated use.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients Aqua (Water), Carthamus Tinctorius (Safflower) Oleosomes, Polyacrylate Cross Polymer - 6 Hydroxyethyl Cellulose, Glycerin.

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 to help reduce bacteria on the skin. Recommended for repeated use


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

Spl product data elements

Usually a list of ingredients in a drug product.

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.

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. Children should only use this product under adult supervision

Other safety information

Information about safe use and handling of the product that may not have been specified in another field.
Other information • Do not store above 104˚F (40˚C). May discolor some fabrics · harmful to wood finishes and plastics


A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.
(800) 621-2079.


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 Flammable. Keep away from fire or flame For external use only Discontinue use if irritation or redness develops. If condition persists for more than 72 hours, consult a doctor. When using this product avoid contact with eyes · In case of contact, flush eyes with water, call a doctor · Avoid contact with broken skin Do not drink. Not edible . In case of accidental ingeston seek professional assistance or contact a Poison Contro 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