Label: VISINE ALLERGY EYE RELIEF MULTI-ACTION- naphazoline hydrochloride and pheniramine maleate solution/ drops
- NDC Code(s): 69968-0367-1, 69968-0367-2
- Packager: Kenvue Brands LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: New Drug Application
Drug Label Information
Updated November 13, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- Uses
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Warnings
For external use only
Ask a doctor before use if you have
- heart disease
- high blood pressure
- narrow angle glaucoma
- trouble urinating
When using this product
- pupils may become enlarged temporarily causing light sensitivity
- do not touch tip of container to any surface to avoid contamination
- replace cap after each use
- remove contact lenses before using
- do not use if this solution changes color or becomes cloudy
- overuse may cause more eye redness
- some users may experience a brief tingling sensation
- Directions
- Other information
- Inactive ingredients
- Questions?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 15 mL Bottle Carton
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INGREDIENTS AND APPEARANCE
VISINE ALLERGY EYE RELIEF MULTI-ACTION
naphazoline hydrochloride and pheniramine maleate solution/ dropsProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69968-0367 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NAPHAZOLINE HYDROCHLORIDE (UNII: MZ1131787D) (NAPHAZOLINE - UNII:H231GF11BV) NAPHAZOLINE HYDROCHLORIDE 0.25 mg in 1 mL PHENIRAMINE MALEATE (UNII: NYW905655B) (PHENIRAMINE - UNII:134FM9ZZ6M) PHENIRAMINE MALEATE 3 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 HYDROXIDE (UNII: 55X04QC32I) HYDROCHLORIC ACID (UNII: QTT17582CB) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69968-0367-1 1 in 1 CARTON 05/06/2019 1 15 mL in 1 BOTTLE; Type 4: Device Coated/Impregnated/Otherwise Combined with Drug 2 NDC:69968-0367-2 2 in 1 CARTON 06/03/2019 2 15 mL in 1 BOTTLE; Type 4: Device Coated/Impregnated/Otherwise Combined with Drug Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NDA NDA020485 05/06/2019 Labeler - Kenvue Brands LLC (118772437)