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El valle decolorized iodine - Medication Information

Product NDC Code 55758-374
Drug Name

El valle decolorized iodine

Type Brand
Active Ingredients
Alcohol .48 mg/ml
Route TOPICAL
Dosage Form TINCTURE
Application Number M004
Labeler Name Pharmadel LLC
Packages
Package NDC Code Description
55758-374-02 30 ml in 1 bottle, plastic (55758-374-02)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredient & Purpose Gentian Violet 1% Active ingredient Purpose Alcohol 48% ............................. First aid antiseptic
Active ingredientPurpose
Alcohol 48% .............................First aid 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.
Directions clean the affected area apply a small amount directly to the affected area 1 to 3 times a day may cover area with sterile bandage

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients ammonia, iodine, sodium iodide, 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 burns

Purpose

Information about the drug product’s indications for use.
Active ingredient Purpose Alcohol 48% ............................. First aid antiseptic
Active ingredientPurpose
Alcohol 48% .............................First aid antiseptic

Spl product data elements

Usually a list of ingredients in a drug product.
El Valle Decolorized Iodine Alcohol AMMONIA WATER ALCOHOL ALCOHOL SODIUM IODIDE IODINE

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.
Prinicpal Display Panel PDP D IODINE

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 Drug facts

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 you have a deep or puncture wounds serious burns animal bites

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 longer than 1 week, unless directed by a doctor in the eyes over large areas of the body

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.

Other safety information

Information about safe use and handling of the product that may not have been specified in another field.
Other information do not use if clear seal over cap is missing or broken

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 consult a doctor if conditions persist or gets worse

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 longer than 1 week, unless directed by a doctor in the eyes over large areas of the body Ask a doctor before use if you have a deep or puncture wounds serious burns animal bites Stop use and consult a doctor if conditions persist or gets worse Keep out of reach of children. If swallowed, get medical help, or contact a Poison Control Center immediately.

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