Label: ATROPINE SULFATE- atropine sulfate ointment

  • NDC Code(s): 24208-825-55
  • Packager: Bausch & Lomb Incorporated
  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated June 14, 2017

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  • DESCRIPTION:

     Atropine Sulfate Ophthalmic Ointment, 1% is a sterile topical anticholinergic for ophthalmic use. The active ingredient is represented by the chemical structural formula:

    chem_structure.jpg

    (C17H23NO3)2•H2SO4•H2O                                                                     
    Mol. Wt. 694.83

    Chemical Name:

    Benzeneacetic acid, α-(hydroxymethyl)-, 8-methyl-8-azabicyclo-[3.2.1]oct-3-yl ester, endo-(±)-, sulfate (2:1) (salt), monohydrate.

    Each gram contains:

    ACTIVE: Atropine Sulfate, 1% (10 mg); INACTIVES: Lanolin oil, mineral oil, purified water, and white petrolatum.

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  • CHEMICAL PHARMACOLOGY

    The anticholinergic effect of this product blocks the responses of the sphincter muscle of the iris and the accommodative muscle of the ciliary body to cholinergic stimulation, producing pupillary dilation (mydriasis) and paralysis of accommodation (cycloplegia).

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  • INDICATIONS AND USAGE

    For mydriasis and/or cycloplegia. For cycloplegic refraction, for pupillary dilation desired in inflammatory conditions of the iris and uveal tract.

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  • CONTRAINDICATIONS

    This product should not be used in patients with primary glaucoma or a predisposition to narrow anterior chamber angle glaucoma.

    This product should not be used in pediatric patients who have previously had a severe systemic reaction to atropine. This product should not be used in those persons showing hypersensitivity to any component of this preparation.

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  • WARNINGS

    In pediatric patients, use with extreme caution. Excessive use in pediatric patients or in certain individuals with a previous history of susceptibility to belladonna alkaloids may produce systemic symptoms of atropine poisoning. If this occurs, discontinue medication and use appropriate therapy as outlined in OVERDOSAGE.

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  • PRECAUTIONS

    To avoid excessive systemic absorption, the lacrimal sac should be compressed by digital pressure for two to three minutes after instillation. To avoid inducing angle closure glaucoma, an estimation of the depth of the angle of the anterior chamber should be made. Administration of atropine in infants requires great caution.

    Patient Warning:

    Patients should be advised not to drive or engage in other hazardous activities while pupils are dilated. Patients may experience sensitivity to light and should protect eyes in bright illumination during dilation.


    Parents should be warned not to get this preparation in their children’s mouth and to wash their own hands and the child’s hands following administration.

    Carcinogenesis, Mutagenesis, Impairment of Fertility:

    No studies have been conducted in animals or in humans to evaluate the potential of these effects.

    Animal reproduction studies have not been performed with atropine. It is also not known whether atropine can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. Atropine should be given to pregnant women only if clearly needed.

    Pediatric Use:

    See CONTRAINDICATIONS and WARNINGS.

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  • ADVERSE REACTIONS

    Prolonged use may produce local irritation characterized by follicular conjunctivitis, vascular congestion, edema, exudate, and an eczematoid dermatitis. Severe reactions are manifested by hypotension with progressive respiratory depression. Coma and death have been reported in the very young.

    To report SUSPECTED ADVERSE REACTIONS, contact Bausch + Lomb, a division of Valeant Pharmaceuticals North America LLC, at 1-800-321-4576 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

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  • OVERDOSAGE

    Systemic atropine toxicity is manifested by flushing and dryness of the skin (a rash may be present in pediatric patients), blurred vision, a rapid and irregular pulse, fever, abdominal distension in infants, mental aberration (hallucinosis) and loss of neuromuscular coordination.


    Atropine poisoning, although distressing, is rarely fatal, even with large doses of atropine, and is self-limited if the cause is recognized and the atropine medication is discontinued. In severe intoxication, physostigmine salicylate may be administered parenterally to provide more prompt relief of the intoxication. Give physostigmine salicylate as 1-5 mL IV of dilution containing 1 mg in 5 mL of saline. The smaller dose is for pediatric patients, and injection should take not less than 2 minutes. EKG control is advisable. Dosage can be repeated every 5 minutes up to a total dose of 2 mg in pediatric patients and 6 mg in adults every 30 minutes. Physostigmine is contraindicated in hypotensive reactions. Atropine (1 mg) should be available for immediate injection if physostigmine causes bradycardia, convulsions or bronchoconstriction. In pediatric patients, the body surface must be kept moist.


    Use extreme caution when employing short-acting barbiturates to control excitement.

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  • DOSAGE AND ADMINISTRATION

    Apply a small amount of ointment to the conjunctival sac once or twice a day, or as directed by a physician.


    FOR OPHTHALMIC USE ONLY

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  • HOW SUPPLIED

    Atropine Sulfate Ophthalmic Ointment, 1% is supplied in an ophthalmic tip applicator tube in the following size:

    3.5 g tubes – NDC 24208-825-55

    Image 1
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  • STORAGE:

    Store between 15°-25°C (59°-77°F).

    KEEP OUT OF REACH OF CHILDREN

    Bausch + Lomb, a division of Valeant Pharmaceuticals North America LLC
    Bridgewater, NJ 08807 USA

    ©Bausch & Lomb Incorporated

    Rev. 06/2017

    9115202 (Folded)
    9115302 (Flat)

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  • PACKAGE/LABEL PRINCIPAL DISPLAY PANEL

    NDC 24208-825-55

    Atropine

    Sulfate

    Ophthalmic

    Ointment, 1%

    (Sterile)

    FOR OPHTALMIC USE ONLY

    Rx only

    Net. Wt. 1/8 oz. (3.5g)

    BAUSCH + LOMB

    3.5g_carton.jpg
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  • INGREDIENTS AND APPEARANCE
    ATROPINE SULFATE 
    atropine sulfate ointment
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:24208-825
    Route of Administration OPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ATROPINE SULFATE (UNII: 03J5ZE7KA5) (ATROPINE - UNII:7C0697DR9I) ATROPINE SULFATE 10 mg  in 1 g
    Inactive Ingredients
    Ingredient Name Strength
    LANOLIN OIL (UNII: OVV5IIJ58F)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    WATER (UNII: 059QF0KO0R)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:24208-825-55 1 in 1 CARTON 09/30/1990
    1 3.5 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    Unapproved drug other 09/30/1990
    Labeler - Bausch & Lomb Incorporated (196603781)
    Establishment
    Name Address ID/FEI Business Operations
    Bausch & Lomb Incorporated 079587625 MANUFACTURE(24208-825) , LABEL(24208-825) , PACK(24208-825)
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