RYNODERM (UREA) CREAM [SOLUTECH PHARMACEUTICALS LLC]

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RYNODERM (UREA) CREAM [SOLUTECH PHARMACEUTICALS LLC]
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NDC 70350-2626-1
Set ID ce0fdc05-038c-410d-8608-d7cd0a816d7a
Category HUMAN PRESCRIPTION DRUG LABEL
Packager SOLUTECH PHARMACEUTICALS LLC
Generic Name
Product Class
Product Number
Application Number
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  • SPL UNCLASSIFIED SECTION

    Rx only

    For external use only.
    Not for ophthalmic use.

  • RYNODERM Description

    Rynoderm cream is a potent keratolytic emollient which is a gentle, yet potent, tissue softener for skin and/or nails.

    Each gram of Rynoderm Cream contains:

    ACTIVE: 37.5% Urea in a cream base of:

    INACTIVES: Mineral Oil, Stearic Acid, Water, Glycerin, Polysorbate 20, Sepigel 305, Phenoxyethanol, Acrylate Copolymer and Vitamin E

    CHEMISTRY

    Urea is a diamide of carbonic acid with the following chemical structure:

    Chemical Structure

  • RYNODERM - Clinical Pharmacology

    Urea gently dissolves the intercellular matrix which results in loosening the horny layer of skin and shedding scaly skin at regular intervals, thereby softening hyperkeratotic areas. Urea also hydrates and gently dissolves the intercellular matrix of the nail plate, which can result in the softening and eventual debridement of the nail plate.

    PHARMACOKINETICS

    The mechanism of action of topically applied urea is not yet known.

  • INDICATIONS AND USES

    For debridement and promotion of normal healing of hyperkeratotic surface lesions, particularly where healing is retarded by local infection, necrotic tissue, fibrinous or prurient debris or eschar. Urea is useful for the treatment of hyperkeratotic conditions such as dry, rough skin, dermatitis, psoriasis, xerosis, ichthyosis, eczema, keratosis, keratoderma, corns and calluses, as well as damaged, ingrown and devitalized nails.

  • Contraindications

    Rynoderm Cream is contraindicated in patients with known hypersensitivity to any of the listed ingredients.

  • Warnings

    For external use only. Avoid contact with eyes, lips or mucous membranes. Do not use on areas of broken skin.

  • Precautions

    After applying this medication, wash hands and unaffected areas thoroughly. Stop use and ask a doctor if redness or irritation develops. If swallowed, get medical help or contact Poison Control Center right away. KEEP THIS AND ALL MEDICATION OUT OF THE REACH OF CHILDREN.

    PREGNANCY

    Pregnancy Category B

    Animal reproduction studies have revealed no evidence of harm to the fetus, however, there are no adequate and well-controlled studies in pregnant women. Because animal reproduction studies are not always predictive of human response, Rynoderm Cream should be given to a pregnant woman only if clearly needed.

    NURSING MOTHERS

    It is not known whether or not this drug is secreted in human milk. Because many drugs are secreted in human milk, caution should be exercised when Rynoderm Cream is administered to a nursing woman.

  • Adverse Reactions

    Transient stinging, burning, itching or irritation may occur and normally disappear on discontinuing the medication.

  • RYNODERM - Dosage and Administration

    Apply Rynoderm Cream to affected skin twice per day or as directed by a physician. Rub in until completely absorbed. Apply to diseased or damaged nail tissue twice per day or as directed by a physician.

  • How is RYNODERM Supplied

    RYNODERM Cream (37.5% urea) is supplied in:

    142g (5 oz) tube70350-2626-1

    Store at 25°C (77°F); excursion permitted to 15°C - 30°C (59° - 86°F) Protect from freezing. [See USP Controlled Room Temperature.]

  • SPL UNCLASSIFIED SECTION

    Manufactured for:
    Solutech Pharmaceuticals LLC
    Peoria, AZ 85345

    Rx only

  • PRINCIPAL DISPLAY PANEL - 142 gm Tube Label

    NDC 70350-2626-1

    FOR TOPICAL USE ONLY

    RYNODERM
    UREA 37.5% CREAM

    Smooth
    Easily Spreadable

    Rx only

    Solutech
    PHARMACEUTICALS

    Net WT. 5OZ (142 gm)

    PRINCIPAL DISPLAY PANEL - 142 gm Tube Label
  • INGREDIENTS AND APPEARANCE
    RYNODERM 
    urea cream
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:70350-2626
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    UREA (UNII: 8W8T17847W) (UREA - UNII:8W8T17847W) UREA375 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    MINERAL OIL (UNII: T5L8T28FGP)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    SODIUM ACRYLOYLDIMETHYLTAURATE-ACRYLAMIDE COPOLYMER (1:1; 90000-150000 MPA.S) (UNII: 5F4963KLHS)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70350-2626-1142 g in 1 TUBE; Type 0: Not a Combination Product10/27/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    Unapproved drug other10/27/2017
    Labeler - SOLUTECH PHARMACEUTICALS LLC (080040396)
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