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Phytozine ringworm treatment maximum strength - Medication Information

Product NDC Code 71229-101
Drug Name

Phytozine ringworm treatment maximum strength

Type Brand
Active Ingredients
Tolnaftate 1 g/100g
Route TOPICAL
Dosage Form OINTMENT
RxCUI drug identifier 199126
Application Number M005
Labeler Name The Sisquoc Healthcare Corporation
Packages
Package NDC Code Description
71229-101-11 28 g in 1 tube (71229-101-11)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
ACTIVE INGREDIENT TOLNAFTATE 1%

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 For the cure of most ringworm (tinea corporis) and athlete’s foot (tinea pedis). For relief of itching, scaling, cracking, burning, redness, soreness, irritation and discomforts which may accompany these conditions. Wash affected area and dry thoroughly. Apply a layer of PHYTOZINE over the affected area twice daily (morning and night). Allow the cream to dry for at least 3 minutes before covering the affectedarea with clothing. Wash hands after each application to preventthe chance of the infection spreading to other parts of the skin. Most ringworm infections will require between 3-4 weeks of continuous daily treatment before the infection is completely eliminated. Proper use of PHYTOZINE will eliminate most ringworm infections. If the condition persists longer, contact a physician or medical professional.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
INACTIVE INGREDIENTS Water, Prunus Amygdalus Dulcis (Sweet Almond) Oil, Polysorbate-20, Sodium Polyacrylate, Hydrogenated Polydecene, Trideceth-6, Glyceryl Stearate, PEG-100, Stearate, Propylene Glycol, Cetyl Alcohol, Oleth-10 Phosphate, Glycerin, Avena (Oat), Kernel Extract, Aloe Barbadensis Leaf Juice, Actrostaphylos Uva Ursi Leaf Extract, Propolis Extract, Theobroma Cacao (Cocoa) Seed Butter, Rosa Canina Fruit Oil, Camphor, Menthol, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Lavandula Angustifolia (Lavender) Oil, Jasminum Officinale (Jasmine) Oil, Eugenia Caryophyllus (Clove) Leaf Oil, Tocopheryl Acetate, Stearic Acid, Propylene Glycol, Butylene Glycol, Cetyl Hydroxyethylcellulose, Sodium Hydroxide, Phenoxyethanol , Ethylhexylglycerin

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 CURES MOST RINGWORM RELIEVES ITCHING, REDNESS, IRRITATION AND DISCOMFORT WHICH ACCOMPANY THIS CONDITION.

Purpose

Information about the drug product’s indications for use.
PURPOSE ANTIFUNGAL

Spl product data elements

Usually a list of ingredients in a drug product.
PHYTOZINE RINGWORM TREATMENT MAXIMUM STRENGTH TOLNAFTATE WATER ALMOND OIL POLYSORBATE 20 SODIUM POLYACRYLATE (8000 MW) HYDROGENATED POLYDECENE (550 MW) TRIDECETH-6 GLYCERYL MONOSTEARATE PEG-100 STEARATE PROPYLENE GLYCOL CETYL ALCOHOL OLETH-10 PHOSPHATE GLYCERIN OAT ALOE VERA LEAF ARCTOSTAPHYLOS UVA-URSI LEAF PROPOLIS WAX THEOBROMA CACAO WHOLE ROSA CANINA FRUIT OIL CAMPHOR (SYNTHETIC) MENTHOL MELALEUCA ALTERNIFOLIA LEAF LAVANDULA ANGUSTIFOLIA WHOLE JASMINUM OFFICINALE WHOLE CLOVE LEAF OIL .ALPHA.-TOCOPHEROL ACETATE STEARIC ACID BUTYLENE GLYCOL CETYL HYDROXYETHYLCELLULOSE (350000 MW) SODIUM HYDROXIDE PHENOXYETHANOL ETHYLHEXYLGLYCERIN TOLNAFTATE TOLNAFTATE

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.
Label Phytozine Retail Proof 1-17 Insert Phytozine '17

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 RIGHT AWAY.

Other safety information

Information about safe use and handling of the product that may not have been specified in another field.
Store between 20°c to 25°C (68° to 77°F)

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. WHEN USING THIS PRODUCT AVOID CONTACT WITH THE EYES. STOP USE AND ASK A DOCTOR IF IRRITATION OCCURS THERE IS NO IMPROVEMENT WITHIN 4 WEEKS. DO NOT USE ON CHILDREN UNDER 2 YEARS OF AGE UNLESS DIRECTED BY A DOCTOR.

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