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Home > Drugs > Ophthalmic anesthetics > Alcaine > Alcaine Prescribing Information
Ophthalmic anesthetics
https://themeditary.com/pro/alcaine-prescribing-information-14844.html

Alcaine Prescribing Information

Drug Detail:Alcaine (Proparacaine ophthalmic [ proe-par-a-kane-off-thal-mik ])

Drug Class: Ophthalmic anesthetics

Contents
Uses Warnings Before Taking Dosage Side effects Interactions

Alcaine Description

ALCAINE™ (proparacaine hydrochloride ophthalmic solution, USP) 0.5% is a topical local anesthetic for ophthalmic use. The active ingredient is represented by the structural formula:


chemical

Established Name: Proparacaine Hydrochloride
Chemical Name: Benzoic acid, 3-amino-4-propoxy-,2-(diethylamino) ethyl ester, monohydrochloride.
Molecular Weight: 330.85 g/mol

Each mL contains of ALCAINE™ (proparacaine hydrochloride ophthalmic solution, USP) 0.5%:
Active:
proparacaine hydrochloride 5 mg 0.5%. Preservative: benzalkonium chloride (0.01%).
Inactives: glycerin and purified water. The pH may be adjusted with hydrochloric acid and/or sodium hydroxide.

Alcaine - Clinical Pharmacology

ALCAINE™ ophthalmic solution is a rapidly-acting topical anesthetic, with induced anesthesia lasting approximately 10-20 minutes.

Indications and Usage for Alcaine

ALCAINE™ ophthalmic solution is indicated for procedures in which a topical ophthalmic anesthetic is indicated: corneal anesthesia of short duration, e.g. tonometry, gonioscopy, removal of corneal foreign bodies, and for short corneal and conjunctival procedures.

Related/similar drugs

lidocaine ophthalmic, proparacaine ophthalmic, Balanced Salt Solution, Ophthaine, BSS, BSS Plus

Contraindications

ALCAINE™ ophthalmic solution should be considered contraindicated in patients with known hypersensitivity to any of the ingredients of this preparation.

Warnings

NOT FOR INJECTION - FOR TOPICAL OPHTHALMIC USE ONLY. Prolonged use of a topical ocular anesthetic is not recommended. It may produce permanent corneal opacification with accompanying visual loss.

ALCAINE™ ophthalmic solution is indicated for administration under the direct supervision of a healthcare provider. ALCAINE™ ophthalmic solution is not intended for patient self-administration.

Precautions

Carcinogenesis, Mutagenesis, Impairment of Fertility.

Long-term studies in animals have not been performed to evaluate carcinogenic potential, mutagenicity, or possible impairment of fertility in males or females.

Pregnancy:

Animal reproduction studies have not been conducted with ALCAINE™ (proparacaine hydrochloride ophthalmic solution, USP) 0.5%. It is also not known whether proparacaine hydrochloride can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. Proparacaine hydrochloride should be administered to a pregnant woman only if clearly needed.

Nursing Mothers:

It is not known whether this drug is excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when proparacaine hydrochloride is administered to a nursing woman.

Pediatric Use:

Safety and effectiveness of proparacaine hydrochloride ophthalmic solution in pediatric patients have been established. Use of proparacaine hydrochloride is supported by evidence from adequate and well-controlled studies in adults and children over the age of twelve, and safety information in neonates and other pediatric patients.

Geriatric Use:

No overall clinical differences in safety or effectiveness have been observed between the elderly and other adult patients.

Adverse Reactions/Side Effects

Occasional temporary stinging, burning and conjunctival redness may occur with the use of proparacaine. A rare, severe, immediate-type, apparently hyperallergic corneal reaction characterized by acute, intense and diffuse epithelial keratitis, a gray, ground glass appearance, sloughing of large areas of necrotic epithelium, corneal filaments and, sometimes, iritis with descemetitis has been reported.

Allergic contact dermatitis from proparacaine with drying and fissuring of the fingertips has also been reported.

Alcaine Dosage and Administration

Usual Dosage: Removal of foreign bodies and sutures, and for tonometry: 1 to 2 drops (in single instillations) in each eye before operating.

Short Corneal and Conjunctival Procedures: 1 drop in each eye every 5 to 10 minutes for 5 to 7 doses.

NOTE: ALCAINE™ (proparacaine hydrochloride ophthalmic solution, USP) 0.5% should be clear to straw-color. If the solution becomes darker, discard the solution.

How is Alcaine supplied

ALCAINE™ (proparacaine hydrochloride ophthalmic solution, USP) 0.5% is supplied in DROP-TAINER® dispensers as follows:

15 mL NDC 0998-0016-15

Storage:

Bottle must be stored in unit carton to protect contents from light.
Store bottles under refrigeration at 2°C to 8°C (36°F to 46°F).

After opening, ALCAINE™ can be used until the expiration date on the bottle.

NOTE: ALCAINE™ (proparacaine hydrochloride ophthalmic solution, USP) 0.5% should be clear to straw-color. If the solution becomes darker, discard the solution.

Distributed by:
ALCON LABORATORIES, INC.
Fort Worth, Texas 76134

Revised: 09/2022


Alcon
Alcon Laboratories, Inc.
6201 South Freeway
Fort Worth, Texas 76134 USA

© 2022 Alcon Inc.
Printed in USA
[email protected]
1-800-757-9195


300056034-0222

PRINCIPAL DISPLAY PANEL

NDC 0998-0016-15

Alcon

Alcaine™
(proparacaine hydrochloride ophthalmic solution USP) 0.5%

15 mL Sterile

Rx Only

PRECAUTION:
NOT FOR INJECTION. FOR TOPICAL OPHTHALMIC USE ONLY. Do not touch dropper tip to any surface, as this may contaminate the solution.

USUAL DOSAGE: 1 or 2 drops. Read enclosed insert.

Bottles must be stored in unit carton to protect from light.

STORAGE: Store between 2º to 8ºC (36º to 46ºF). After opening, ALCAINE™ can be used until the expiration date on the bottle.

ALCAINE™ (proparacaine hydrochloride ophthalmic solution) should be clear to straw-color. If the solution becomes darker, discard the solution.

INGREDIENTS: Each mL contains: Active: proparacaine hydrochloride 5 mg (0.5%). Preservative: benzalkonium chloride 0.01%. Inactives: glycerin, hydrochloric acid and/or sodium hydroxide (to adjust pH), purified water

pH range 4.0 to 6.0

1-800-757-9195
[email protected]
Country of Origin: Switzerland

Alcon
ALCON LABORATORIES, INC.
6201 South Freeway
Fort Worth, Texas 76134 USA
Printed in USA
300056033-0922

Carton Label

NDC 0998-0016-15

Alcon

Alcaine®
(proparacaine hydrochloride ophthalmic solution USP) 0.5%

15 mL Sterile

Rx Only

PRECAUTION:
NOT FOR INJECTION. FOR TOPICAL OPHTHALMIC USE ONLY. Do not touch dropper tip to any surface, as this may contaminate the solution.

USUAL DOSAGE: 1 or 2 drops. Read enclosed insert.

Bottles must be stored in unit carton to protect from light.

STORAGE: Store between 2º-8ºC (36º-46ºF).

ALCAINE® (proparacaine hydrochloride ophthalmic solution) should be clear to straw-color. If the solution becomes darker, discard the solution.

INGREDIENTS: Each mL contains: Active: proparacaine hydrochloride 5 mg (0.5%). Preservative: benzalkonium chloride 0.01%. Inactives: glycerin, hydrochloric acid and/or sodium hydroxide (to adjust pH), purified water

pH range 4.0 to 6.0

1-800-757-9195
[email protected]
Country of Origin: Switzerland

Alcon
ALCON LABORATORIES, INC.
6201 South Freeway
Fort Worth, Texas 76134 USA
Printed in USA
300048624-0721

Carton Label

NDC 0998-0016-15

Alcon

Alcaine®
(proparacaine hydrochloride ophthalmic solution USP) 0.5%

15 mL Sterile

Rx Only

PRECAUTION:
NOT FOR INJECTION. FOR TOPICAL OPHTHALMIC USE ONLY. Do not touch dropper tip to any surface, as this may contaminate the solution.

USUAL DOSAGE: 1 or 2 drops. Read enclosed insert.

Bottles must be stored in unit carton to protect from light.

STORAGE: Store between 2º-8ºC (36º-46ºF).

ALCAINE® (proparacaine hydrochloride ophthalmic solution) should be clear to straw-color. If the solution becomes darker, discard the solution.

INGREDIENTS: Each mL contains: Active: proparacaine hydrochloride 5 mg (0.5%). Preservative: benzalkonium chloride 0.01%. Inactives: glycerin, hydrochloric acid and/or sodium hydroxide (to adjust pH), purified water

pH range 4.0 to 6.0

1-800-757-9195
[email protected]
Country of Origin: Switzerland

Alcon
ALCON LABORATORIES, INC.
6201 South Freeway
Fort Worth, Texas 76134 USA
Printed in USA
9016948-0119

SN:

LOT:

EXP:

GTIN: 00309980016156

carton

NDC 0998-0016-15

Alcon

Alcaine™
(proparacaine hydrochloride ophthalmic solution USP) 0.5%

Sterile 15 mL

Rx Only

PRECAUTION:
NOT FOR INJECTION. FOR TOPICAL OPHTHALMIC USE ONLY. Do not touch dropper tip to any surface as this may contaminate the solution.

USUAL DOSAGE: 1 or 2 drops. Read enclosed insert.

STORAGE: Store between 2º to 8ºC (36º to 46ºF).
After opening, ALCAINE™ can be used until the expiration date on the bottle.

Bottles must be stored in unit carton to protect from light.

ALCAINE™ (proparacaine hydrochloride ophthalmic solution) should be clear to straw-color. If the solution becomes darker, discard the solution.


INGREDIENTS: Each mL contains: Active: proparacaine hydrochloride 5 mg (0.5%).


ALCON LABORATORIES, INC.
Fort Worth, Texas 76134 USA Printed in USA

LOT/EXP.:

Container Label

NDC 0998-0016-15

Alcon

Alcaine®
(proparacaine hydrochloride ophthalmic solution USP) 0.5%

Sterile 15 mL

Rx Only

PRECAUTION:
NOT FOR INJECTION. FOR TOPICAL OPHTHALMIC USE ONLY. Do not touch dropper tip to any surface as this may contaminate the solution.

USUAL DOSAGE: 1 or 2 drops. Read enclosed insert.

STORAGE: Store between 2º-8ºC (36º-46ºF).

Bottles must be stored in unit carton to protect from light.

ALCAINE® (proparacaine hydrochloride ophthalmic solution) should be clear to straw-color. If the solution becomes darker, discard the solution.


INGREDIENTS: Each mL contains: Active: proparacaine hydrochloride 5 mg (0.5%).


ALCON LABORATORIES, INC.
Fort Worth, Texas 76134 USA Printed in USA


LOT/EXP.:

Container Label

NDC 0998-0016-15

Alcon

Alcaine®
(proparacaine hydrochloride ophthalmic solution USP) 0.5%

Sterile 15 mL

Rx Only

PRECAUTION:
NOT FOR INJECTION. FOR TOPICAL OPHTHALMIC USE ONLY. Do not touch dropper tip to any surface as this may contaminate the solution.

USUAL DOSAGE: 1 or 2 drops. Read enclosed insert.

STORAGE: Store between 2º-8ºC (36º-46ºF).

Bottles must be stored in unit carton to protect from light.

ALCAINE® (proparacaine hydrochloride ophthalmic solution) should be clear to straw-color. If the solution becomes darker, discard the solution.


INGREDIENTS: Each mL contains: Active: proparacaine hydrochloride 5 mg (0.5%).


ALCON LABORATORIES, INC.
Fort Worth, Texas 76134 USA Printed in USA
A Novartis Division


LOT/EXP.:

H15466-1118

label

ALCAINE
proparacaine hydrochloride solution/ drops
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:0998-0016
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PROPARACAINE HYDROCHLORIDE (UNII: U96OL57GOY) (PROPARACAINE - UNII:B4OB0JHI1X) PROPARACAINE HYDROCHLORIDE5 mg in 1 mL
Inactive Ingredients
Ingredient NameStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0998-0016-151 in 1 CARTON10/19/1973
115 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA08002710/19/1973
Labeler - Alcon Laboratories, Inc. (008018525)
Registrant - Alcon Laboratories, Inc. (008018525)
Establishment
NameAddressID/FEIBusiness Operations
Alcon Research, LLC007672236manufacture(0998-0016)

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