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Target up and up 2-in-1 hand sanitizer - Medication Information

Product NDC Code 11673-147
Drug Name

Target up and up 2-in-1 hand sanitizer

Type Brand
Active Ingredients
Benzalkonium chloride 1.3 mg/ml
Route TOPICAL
Dosage Form LOTION
RxCUI drug identifier 1046442
Application Number M003
Labeler Name TARGET CORPORATION
Packages
Package NDC Code Description
11673-147-15 150 ml in 1 tube (11673-147-15)
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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 Apply product to hands. Rub hands together until absorbed. Do not wipe off or rinse. Apply to hands as needed.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients Water, Glycerin, Distearyldimonim Chloride, Isopropyl Palmitate, Aloe Barbadensis Leaf Juice, Theobroma Cacao (Cocoa) Seed Butter, Butyrospermum Parkii (Shea) Btter, Dimethicone, Steareth-20, Magnesium Silicate, Fragrance, Alcohol, Phenoxyethanol.

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 helps decrease bacteria on the hands

Purpose

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

Spl product data elements

Usually a list of ingredients in a drug product.
Target Up and Up 2-in-1 Hand Sanitizer BENZETHONIUM CHLORIDE STEARETH-20 SHEA BUTTER GLYCERIN BENZALKONIUM CHLORIDE BENZALKONIUM WATER ALOE VERA LEAF COCOA BUTTER PHENOXYETHANOL MAGNESIUM ALUMINUM SILICATE DISTEARYLDIMONIUM CHLORIDE CETYL ALCOHOL ALCOHOL DIMETHICONE ISOPROPYL PALMITATE

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.
82035A

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 on infants under 6 months of age

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 except under adult supervision. If swallowed, get medical help or contact a Poison Control right away.

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 rash occurs.

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 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

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