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Sterile alcohol prep pads 01 - Medication Information

Product NDC Code 55550-222
Drug Name

Sterile alcohol prep pads 01

Type Brand
Active Ingredients
Isopropyl alcohol .7 ml/ml
Route TOPICAL
Dosage Form SWAB
RxCUI drug identifier 797544
Application Number part333A
Labeler Name Total Resources International Inc.
Packages
Package NDC Code Description
55550-222-01 1.4 ml in 1 pouch (55550-222-01)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredients Isopropyl Alcohol 70% v/v Purpose Antiseptic

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.
Alcohol Prep Pad 1 Pad Manufactured by: Total Resources International Inc. Walnut, California 91789 Made in China REORDER NO: 00-ALC-90730COM

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredient 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.
Directions Apply to skin as needed and discard after single use

Purpose

Information about the drug product’s indications for use.
Use First aid to help prevent infection in minor cuts and scrapes For preparation of the skin prior to an injection

Spl product data elements

Usually a list of ingredients in a drug product.
STERILE ALCOHOL PREP PADS 01 isopropyl alcohol WATER ISOPROPYL ALCOHOL ISOPROPYL ALCOHOL

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.
Front Label Back Label

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, If contact occurs, flush eyes with water with electrocautery procedures

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 Immediately.

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

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