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Pacific blue ultra foaming fragrance free - Medication Information

Product NDC Code 54622-122
Drug Name

Pacific blue ultra foaming fragrance free

Type Brand
Active Ingredients
Alcohol 70 mg/ml
Route TOPICAL
Dosage Form SOLUTION
RxCUI drug identifier 616805
Application Number 505G(a)(3)
Labeler Name Georgia-Pacific Consumer Products LP
Packages
Package NDC Code Description
54622-122-01 1000 ml in 1 bottle, dispensing (54622-122-01)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredient Ethyl 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 Wet hands thoroughly with product and allow to dry without wiping.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients Water, Isopropyl Alcohol, PEG-12 Dimethicone, Glycerin, Caprylic/Capric Triglyceride, Isopropyl Myristate

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 To decrease bacteria on skin that could cause disease Recommended for repeated use

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.
Pacific Blue Ultra Foaming Fragrance Free Ethyl Alcohol WATER ISOPROPYL ALCOHOL PEG-12 DIMETHICONE GLYCERIN GLYCERYL CAPRYLATE/CAPRATE ISOPROPYL MYRISTATE ALCOHOL 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.
principal display panel Foam Hand Sanitizer 1000 mL (33.8 FL OZ) container label container labelPBb container labelPBAb

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.
Additional rear label text Pacific Blue Ultra Foam Hand Sanitizer Fragrance Free SKU 43335 Manufactured for Georgia-Pacific Consumer Products. Atlanta, GA 30303 Quesitons? Call 1-866-HELLOGP (435-5647) or visit us online at www.gppro.com (c) 2019 GP PRO. All rights reserved. alcohol permit SDS-KY-15002 43335-B2 PRD Rev A

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, seek immediate medical attention or call a poison control center.

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 redness develops. If condition persists for more than 72 hours consult a doctor.

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 use in or near eyes.

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 FLAMMABLE, keep away from fire and flame 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