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Tinfu isopropyl alcohol prep pads - Medication Information

Product NDC Code 82167-000
Drug Name

Tinfu isopropyl alcohol prep pads

Type Brand
Active Ingredients
Isopropyl alcohol .7 ml/ml
Route TOPICAL
Dosage Form CLOTH
RxCUI drug identifier 797544
Application Number M003
Labeler Name Shandong T&F Medical Technology Co., Ltd
Packages
Package NDC Code Description
82167-000-01 .12 ml in 1 patch (82167-000-01)
82167-000-02 100 packet in 1 box (82167-000-02) / .12 ml in 1 packet
82167-000-03 200 packet in 1 box (82167-000-03) / .12 ml in 1 packet
82167-000-04 300 packet in 1 box (82167-000-04) / .12 ml in 1 packet
82167-000-05 .25 ml in 1 patch (82167-000-05)
82167-000-06 100 packet in 1 box (82167-000-06) / .25 ml in 1 packet
82167-000-07 200 packet in 1 box (82167-000-07) / .25 ml in 1 packet
82167-000-08 300 packet in 1 box (82167-000-08) / .25 ml in 1 packet
82167-000-09 .56 ml in 1 patch (82167-000-09)
82167-000-10 100 packet in 1 box (82167-000-10) / .56 ml in 1 packet
82167-000-11 200 packet in 1 box (82167-000-11) / .56 ml in 1 packet
82167-000-12 300 packet in 1 box (82167-000-12) / .56 ml in 1 packet
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredient(s) Isopropyl Alcohol, 70% 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 Apply to skin as needed. Discard after single use.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients 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.
Use For preparation of the skin prior to injection.

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.
Tinfu Isopropyl Alcohol Prep Pads 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.
Package Label - Principal Display Panel NDC: 82167-000 Label

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.
This is a hand sanitizer manufactured according to the Temporary Policy for Preparation of Certain Alcohol-Based Hand Sanitizer Products During the Public Health Emergency (CoViD-19); Guidance for Industry . The hand sanitizer is manufactured using only the following United States Pharmacopoeia (USP) grade ingredients in the preparation of the product (percentage in final product formulation) consistent with World Health Organization (WHO) recommendations: Isopropyl Alcohol (75%, v/v) in an aqueous solution denatured according to Alcohol and Tobacco Tax and Trade Bureau regulations in 27 CFR part 20. Glycerol (1.45% v/v). Hydrogen peroxide (0.125% v/v). Sterile distilled water or boiled cold water. The firm does not add other active or inactive ingredients. Different or additional ingredients may impact the quality and potency of the product. If pregnant or breastfeeding ask a health professional before use.

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 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 accidentally swallowed, get medical help or contact a Poison Control Center 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 and redness develops.

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 do not get into eyes. do not apply over large areas of the body. in case of deep or puncture wounds, animal bites or serious burns, consult a doctor. use only in a well ventilated area.

Storage and handling

Information about safe storage and handling of the drug product.
Other information Store at room temperature 15-30C (59-86F)

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