Label: EYE ALLERGY RELIEF- naphazoline hydrochloride and pheniramine maleate solution/ drops
- NDC Code(s): 69842-441-02, 69842-441-15
- Packager: CVS PHARMACY
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: New Drug Application
Drug Label Information
Updated March 4, 2020
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- Official Label (Printer Friendly)
- Active Ingredients
- Purpose
- Uses
-
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?
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Package/Label Principal Display Panel
CVS
HealthTMEye Allergy Relief
pheniramine maleate 0.315%
Naphazoline hydrochloride 0.02675%
EYE DROPS
Relieves itching & redness caused by:
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- Pollen, grass & ragweed
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- Animal hair & dander
TWIN
PACK[two bottle icon]
[teardrop icon]Actual Product
Size on Side Panel
STERILE
2 BOTTLES
0.5 FL OZ (15 ml) EACH -
INGREDIENTS AND APPEARANCE
EYE ALLERGY RELIEF
naphazoline hydrochloride and pheniramine maleate solution/ dropsProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69842-441 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) WATER (UNII: 059QF0KO0R) SODIUM BORATE (UNII: 91MBZ8H3QO) SODIUM CHLORIDE (UNII: 451W47IQ8X) HYDROCHLORIC ACID (UNII: QTT17582CB) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69842-441-15 1 in 1 CARTON 02/01/2017 1 15 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 2 NDC:69842-441-02 2 in 1 CARTON 02/01/2017 2 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 02/01/2017 Labeler - CVS PHARMACY (062312574) Establishment Name Address ID/FEI Business Operations Bausch & Lomb Incorporated 079587625 MANUFACTURE(69842-441)