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Latisse 0.03% Drops 3 Ml By Allergan Inc

Image 0 of Latisse 0.03% Drops 3 Ml By Allergan IncImage 1 of Latisse 0.03% Drops 3 Ml By Allergan Inc

Latisse 0.03% Drops 3 Ml By Allergan Inc

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Latisse 0.03% Drops 3 Ml By Allergan Inc This Item Requires A Valid Order From A Physician Licensed in USA. Item Number.:RXB10125761/RXD4915658/RXA601205
Size : 3 ML
Selling UoM : EA
NDC: 00023-3616-70
UPC Barcode : 300233616703
Supplier: 0050001063 ALLERGAN USA, INC.
Supplier Material : 361670
Generic Code : 064746 BIMATOPROST TOPICAL DROP W/APP 0.03 %
Fine Line Class : 850085008510 All Rx Products
Product Category : RX Pharmaceuticals
Product Type : BRX Branded RX

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Product Description.:

Drops , clear , clear

LATISSE? solution is a prescription treatment for hypotrichosis used to grow eyelashes, making them longer, thicker and darker.
Eyelash hypotrichosis is another name for having inadequate or not enough eyelashes.

Important Safety Information
If you are using prescription products for lowering eye pressure or have a history of eye pressure problems, only use LATISSE? under close doctor supervision. May cause eyelid skin darkening which may be reversible, and there is potential for increased brown iris pigmentation which is likely to be permanent. There is a potential for hair growth to occur in areas where LATISSE? solution comes in repeated contact with skin surfaces. If you develop or experience any eye problems or have eye surgery, consult your doctor immediately about continued use of LATISSE?. The most common side effects after using LATISSE? solution are an itching sensation in the eyes and/or eye redness.
Possible side effects.

The most common side effects after using LATISSE? solution are an itching sensation in the eyes and/or eye redness. This was reported in approximately 4% of patients. LATISSE? solution may cause other less common side effects which typically occur on the skin close to where LATISSE? is applied, or in the eyes. These include skin darkening, eye irritation, dryness of the eyes, and redness of the eyelids.

If you develop a new ocular condition (e.g., trauma or infection), experience a sudden decrease in visual acuity, have ocular surgery, or develop any ocular reactions, particularly conjunctivitis and eyelid reactions, you should immediately seek your physician's advice concerning the continued use of LATISSE? solution.
Special warnings associated with LATISSE? use.

LATISSE? solution is intended for use on the skin of the upper eyelid margins at the base of the eyelashes. Refer to the illustration below. DO NOT APPLY to the lower eyelid. If you are using LUMIGAN? or other products in the same class for elevated intraocular pressure (IOP), or if you have a history of abnormal IOP, you should only use LATISSE? under the close supervision of your physician.

LATISSE? use may cause darkening of the eyelid skin which may be reversible. LATISSE? use may also cause increased brown pigmentation of the colored part of the eye which is likely to be permanent.

It is possible for hair growth to occur in other areas of your skin that LATISSE? frequently touches. Any excess solution outside the upper eyelid margin should be blotted with a tissue or other absorbent material to reduce the chance of this from happening. It is also possible for a difference in eyelash length, thickness, fullness, pigmentation, number of eyelash hairs, and/or direction of eyelash growth to occur between eyes. These differences, should they occur, will usually go away if you stop using LATISSE?.
Other Important Safety Information

DO NOT APPLY in your eye or to the lower lid. ONLY use the sterile applicators supplied with LATISSE? to apply the product.

Don't allow the tip of the bottle or applicator to contact surrounding structures, fingers, or any other unintended surface in order to avoid contamination by common bacteria known to cause infections.

Contact lenses should be removed prior to application of LATISSE? and may be reinserted 15 minutes following its administration.

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