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Drug Product Composition: Benoxinate Hydrochloride

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USFDA APPLICATION NUMBER - 211039 / DOSAGE - SOLUTION/DROPS;OPHTHALMIC - 0.4%;0.3%

Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BENOXINATE HYDROCHLORIDE(UNII: 0VE4U49K15)
(BENOXINATE - UNII:AXQ0JYM303)
BENOXINATE HYDROCHLORIDE4.4mg in 1
FLUORESCEIN SODIUM(UNII: 93X55PE38X)
(FLUORESCEIN - UNII:TPY09G7XIR)
FLUORESCEIN SODIUM2.6mg in 1

Inactive Ingredients

Ingredient Name
Bausch & Lomb Americas Inc.
BORIC ACID(R57ZHV85D4)
POVIDONE, UNSPECIFIED(FZ989GH94E)
WATER(059QF0KO0R)