, zinc chloride), sodium hydroxide and/or hydrochloric acid to adjust pH, and purified water, USP. Preserved in the bottle with an ionic buffered system, sofZia®.
DROP-TAINER® Dispenser
STORAGE: Store at 2º-25ºC (36º-77°F).
FOR TOPICAL OPHTHALMIC USE
USUAL DOSAGE: Instill one drop in the affected eye(s) once daily in the evening.
© Novartis
ALCON LABORATORIES, INC.
6201 South Freeway
Fort Worth, TX 76134 USA
1-800-757-9195
MedInfo@Alcon.com
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INGREDIENTS AND APPEARANCE
TRAVATAN Z
travoprost solution/ drops
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0065-0260
Route of Administration OPHTHALMIC
Active Ingredient/Active Moiety
Ingredient Name
Basis of Strength
Strength
TRAVOPROST (UNII: WJ68R08KX9) (TRAVOPROST - UNII:WJ68R08KX9) TRAVOPROST 0.04 mg in 1 mL
Inactive Ingredients
Ingredient Name
Strength
POLYOXYL 40 CASTOR OIL (UNII: 4ERD2076EF)
BORIC ACID (UNII: R57ZHV85D4)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
SORBITOL (UNII: 506T60A25R)
ZINC CHLORIDE (UNII: 86Q357L16B)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
HYDROCHLORIC ACID (UNII: QTT17582CB)
WATER (UNII: 059QF0KO0R)
Packaging
#
Item Code
Package Description
Marketing Start Date
Marketing End Date
1 NDC:0065-0260-25 1 in 1 CARTON 10/20/2006
1 2.5 mL in 1 BOTTLE; Type 0: Not a Combination Product
2 NDC:0065-0260-05 1 in 1 CARTON 10/20/2006
2 5 mL in 1 BOTTLE; Type 0: Not a Combination Product
3 NDC:0065-0260-02 1 in 1 CARTON 10/20/2006
3 2.5 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing Category
Application Number or Monograph Citation
Marketing Start Date
Marketing End Date
NDA NDA021994 10/20/2006
Labeler - Alcon Laboratories, Inc (008018525)
Registrant - Alcon Research Ltd (007672236)
Establishment
Name
Address
ID/FEI
Business Operations
Alcon Research Ltd 007672236 MANUFACTURE(0065-0260)
Establishment
Name
Address
ID/FEI
Business Operations
S.A. Alcon-Couvreur N.V. 370205429 manufacture(0065-0260)
