Label: EYE ALLERGY RELIEF- pheniramine maleate and naphazoline hydrochloride solution/ drops
- NDC Code(s): 11673-430-15
- Packager: Target Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: New Drug Application
Drug Label Information
Updated November 22, 2021
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- Active ingredients
- Purpose
- Uses
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Warnings
For external use only
Do not use
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- if you are sensitive to any ingredient in this product
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- if solution changes color or becomes cloudy
Ask a doctor before use if you have
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- heart disease
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- high blood pressure
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- trouble urinating due to an enlarged prostate gland
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- narrow angle glaucoma
When using this product
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- overuse may cause more eye redness
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- pupils may become enlarged temporarily
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- do not touch tip of container to any surface to avoid contamination
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- you may feel a brief tingling after putting drops in eye
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- replace cap after use
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- remove contact lenses before using
- Directions
- Other information
- Inactive ingredients
- Questions or Comments?
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Package/Label Principal Display Panel
NDC 11673-430-15
Compare to active ingredient
in Opcon-A*eye allergy
relief dropsPheniramine Maleate 0.315%
and Naphazoline Hydrochloride
0.02675% Ophthalmic SolutionITCHING AND REDNESS
RELIEVER EYE DROPSrelieves itching and redness caused
by grass, ragweed, pollen, animal hair
and dander[drop icon]
[arrow icon] up & up™STERILE 0.5 FL OZ (15 mL)
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INGREDIENTS AND APPEARANCE
EYE ALLERGY RELIEF
pheniramine maleate and naphazoline hydrochloride solution/ dropsProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11673-430 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NAPHAZOLINE HYDROCHLORIDE (UNII: MZ1131787D) (NAPHAZOLINE - UNII:H231GF11BV) NAPHAZOLINE HYDROCHLORIDE 0.2675 mg in 1 mL PHENIRAMINE MALEATE (UNII: NYW905655B) (PHENIRAMINE - UNII:134FM9ZZ6M) PHENIRAMINE MALEATE 3.15 mg in 1 mL Inactive Ingredients Ingredient Name Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) BORIC ACID (UNII: R57ZHV85D4) EDETATE DISODIUM (UNII: 7FLD91C86K) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) WATER (UNII: 059QF0KO0R) SODIUM BORATE (UNII: 91MBZ8H3QO) SODIUM CHLORIDE (UNII: 451W47IQ8X) HYDROCHLORIC ACID (UNII: QTT17582CB) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11673-430-15 1 in 1 CARTON 08/31/2010 1 15 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NDA NDA020065 08/31/2010 Labeler - Target Corporation (006961700) Registrant - Bausch & Lomb Incorporated (196603781) Establishment Name Address ID/FEI Business Operations Bausch & Lomb Incorporated 114406598 MANUFACTURE(11673-430) Establishment Name Address ID/FEI Business Operations Bausch & Lomb Incorporated 079587625 MANUFACTURE(11673-430)