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Hydrogen peroxide - Medication Information

Product NDC Code 61010-5400
Drug Name

Hydrogen peroxide

Type Generic
Active Ingredients
Hydrogen peroxide 30 mg/ml
Route TOPICAL
Dosage Form SPRAY
RxCUI drug identifier 283420
Application Number M003
Labeler Name Safetec of America, Inc.
Packages
Package NDC Code Description
61010-5400-2 59.1 ml in 1 bottle, spray (61010-5400-2)
61010-5400-4 118 ml in 1 bottle, spray (61010-5400-4)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredients Hydrogen Peroxide 3.0%

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 spray over affected area if bandaged, let dry first

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients 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 First aid to help prevent infection in minor cuts, scrapes and burns

Purpose

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

Spl product data elements

Usually a list of ingredients in a drug product.
Hydrogen Peroxide Hydrogen Peroxide WATER HYDROGEN PEROXIDE HYDROGEN PEROXIDE

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 – 2 oz. bottle label NDC 61010-5400-2 Safetec Hydrogen Peroxide Spray First Aid to Help Prevent Infection in Minor Cuts, Scrapes and Burns. 2 fl. oz. (59.1ml) Reorder no. 53001 PRINCIPAL DISPLAY PANEL – 2 oz. bottle 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.
Drug Facts

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 near eyes or mucous membranes on deep or puncture wounds, animal bites, or serious burns

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. Caution not for use on large areas of the body if redness, irritation, swelling or pain persists or increases, discontinue use and consult a physician

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. Do not use near eyes or mucous membranes on deep or puncture wounds, animal bites, or serious burns Keep out of reach of children. Caution not for use on large areas of the body if redness, irritation, swelling or pain persists or increases, discontinue use and consult a physician

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