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Medline - Medication Information

Product NDC Code 53329-133
Drug Name

Medline

Type Brand
Active Ingredients
Alcohol 62 ml/100ml
Route TOPICAL
Dosage Form SWAB
RxCUI drug identifier 1041780
Application Number 505G(a)(3)
Labeler Name Medline Industries, LP
Packages
Package NDC Code Description
53329-133-27 10 packet in 1 box (53329-133-27) / 6 ml in 1 packet (53329-133-78)
53329-133-78 6 ml in 1 packet (53329-133-78)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredient Ethyl alcohol 62% v/v

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 1. use a tissue to clean the inside of both nostrils, including the inside tip of nostril. Discard 2. insert swab comfortably into tip of right nostril and rotate for 30 seconds, covering all surfaces 3. using same swab, repeat step 2 with tip of left nostril 4. do not blow nose. If solution drips, gently wipe with a tissue directions

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients ascorbyl palmitate, benzyl alcohol, BHT, ricinus communis (castor) seed oil, fragrance, isopropyl alcohol, menthol, polyaminopropyl biguanide, purified water

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 • helps reduce bacteria that can cause skin infections

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.
Medline ethyl alcohol MENTHOL ALCOHOL ALCOHOL ASCORBYL PALMITATE CASTOR OIL ISOPROPYL ALCOHOL BENZYL ALCOHOL BUTYLATED HYDROXYTOLUENE WATER POLYAMINOPROPYL BIGUANIDE

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 Label Label V2 RJ21APL front Label V2 RJ21APL back

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.
Manufacturing Information Manufactured by: Medline Industries, LP Three Lakes Drive, Northfield, IL 60093 USA Made in USA 1-800-MEDLINE (633-5463) REF: MDSR1971 V2 RJ21APL

Ask doctor

Information about when a doctor should be consulted about existing conditions or sumptoms before using the drug product, including all warnings for persons with certain preexisting conditions (excluding pregnancy) and all warnings for persons experiencing certain symptoms. The warnings under this heading are those intended only for situations in which consumers should not use the product until a doctor is consulted.
Ask a doctor before use if injuries are • deep or puncture wounds • serious burns

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 • in the eyes • on children under 2 years of age unless directed by a doctor

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 accidentally swallowed, seek medical assistance or immediately contact a Poison Control Center.

Other safety information

Information about safe use and handling of the product that may not have been specified in another field.
Other information • protect from freezing and avoid excessive heat • not made with natural rubber latex

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 • redness, irritation, swelling or pain persists or increases • infection occurs

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. Flammable, keep away from fire or flame. Do not use • in the eyes • on children under 2 years of age unless directed by a doctor Ask a doctor before use if injuries are • deep or puncture wounds • serious burns Stop use and ask a doctor if • redness, irritation, swelling or pain persists or increases • infection occurs Keep out of reach of children. If accidentally swallowed, seek medical assistance or immediately contact a Poison Control Center.

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