01 2AbbVie Inc
02 1Allergan Aesthetics
03 1Aspen Pharmacare Holdings
04 3Alcon Inc
05 1Altaire Pharmaceuticals
06 1Appasamy Associates
07 5Bausch & Lomb Incorporated
08 1Clear Eyes Pharma Limited
09 1Flagship Biotech International Pvt. Ltd
10 4Hanlim Pharmaceuticals Inc
11 2Johnson & Johnson
12 2Novartis Pharmaceuticals Corporation
13 3Prestige Consumer Healthcare
14 2Raha Pharmaceutical Co
15 2Rising Pharmaceuticals Inc
16 3World Medicine
01 1 Eye Drop
02 3DROPS
03 1EYE AND NOSE DROPS
04 4EYE DROP
05 1EYE DROPS
06 1EYE DROPS, SOLUTION
07 1Eye Drop
08 2LIQUID
09 1NASAL SPRAY
10 1Nasal Spray
11 1OPD
12 1Ophthalmic Drop
13 3SOLUTION
14 13SOLUTION/DROPS;OPHTHALMIC
01 8DISCN
02 9Generic
03 13OTC
04 4Blank
01 2ALBALON
02 1ANC
03 1CLEAR EYES
04 1CLEAR EYES ALLERGY
05 1CLEAR EYES EXTRA STRENGTH REDNESS RELIEF
06 1Cleari
07 1EYEFEEL
08 1MAXIMUM REDNESS RELIEF
09 1Murine Clear Eyes
10 2NAFAZAIR
11 1NAPHAZOLINE HYDROCHLORIDE
12 2NAPHAZOLINE HYDROCHLORIDE AND PHENIRAMINE MALEATE
13 1NAPHCON A
14 1NAPHCON FORTE
15 1NAPHCON-A
16 1NAZOLIN
17 1OPCON
18 1OPCON-A
19 1REDNESS RELIEF
20 1REFRESH EYE ALLERGY RELIEF
21 1SOOTHE ALLERGY
22 1VASOCON
23 1VASOCON-A
24 1VISINE
25 1VISINE FOR ALLERGY WITH ANTIHISTAMINE
26 6Blank
01 8Canada
02 2India
03 2Iran
04 1South Africa
05 4South Korea
06 1Sweden
07 3Turkey
08 13USA
Regulatory Info : OTC
Registration Country : Canada
Brand Name : ALBALON
Dosage Form : DROPS
Dosage Strength : 0.1%/W/V
Packaging : 15ML
Approval Date :
Application Number : 1147
Regulatory Info : OTC
Registration Country : Canada
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ALBALON
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : 0.1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 80248
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : Generic
Registration Country : South Africa
Brand Name : Murine Clear Eyes
Dosage Form : OPD
Dosage Strength : 0.12mg/ml
Packaging : 15X1mg/ml
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Africa
Regulatory Info : OTC
Registration Country : Canada
Brand Name : REFRESH EYE ALLERGY RELIEF
Dosage Form : SOLUTION
Dosage Strength : 0.051%
Packaging : 15ML
Approval Date :
Application Number : 2315890
Regulatory Info : OTC
Registration Country : Canada
Regulatory Info : OTC
Registration Country : USA
NAPHAZOLINE HYDROCHLORIDE; PHENIRAMINE MALEATE
Brand Name : NAPHCON-A
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : 0.025%;0.3%
Packaging :
Approval Date : 1994-06-08
Application Number : 20226
Regulatory Info : OTC
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : NAPHCON FORTE
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : 0.1%
Packaging :
Approval Date : 1982-01-01
Application Number : 80229
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : OTC
Registration Country : Canada
Brand Name : NAPHCON A
Dosage Form : SOLUTION
Dosage Strength : 0.025%
Packaging : 15ML/2.5ML
Approval Date :
Application Number : 481408
Regulatory Info : OTC
Registration Country : Canada
Regulatory Info : OTC
Registration Country : USA
NAPHAZOLINE HYDROCHLORIDE; PHENIRAMINE MALEATE
Brand Name : NAPHAZOLINE HYDROCHLORIDE AND PHENIRAMINE MALEATE
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : 0.02675%;0.315%
Packaging :
Approval Date : 2010-09-27
Application Number : 78208
Regulatory Info : OTC
Registration Country : USA
Regulatory Info :
Registration Country : India
Naphazoline HCl; Chlorpheniramine Maleate; Zinc Sulphate; Hypromellose API; Benzalkonium Chloride
Brand Name : ANC
Dosage Form : Eye Drop
Dosage Strength : 0.56MG; 0.1MG; 12MG; 2MG; 0.0001ML
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info : OTC
Registration Country : USA
NAPHAZOLINE HYDROCHLORIDE; PHENIRAMINE MALEATE
Brand Name : OPCON-A
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : 0.02675%;0.315%
Packaging :
Approval Date : 1994-06-08
Application Number : 20065
Regulatory Info : OTC
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : NAFAZAIR
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : 0.1%
Packaging :
Approval Date : 1994-05-25
Application Number : 40073
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : OPCON
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : 0.1%
Packaging :
Approval Date : 1982-01-01
Application Number : 87506
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : NAFAZAIR
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : 0.1%
Packaging :
Approval Date : 1983-04-15
Application Number : 88101
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : OTC
Registration Country : Canada
Brand Name : SOOTHE ALLERGY
Dosage Form : DROPS
Dosage Strength : 0.02675%/W/V
Packaging : 3ML/15ML
Approval Date :
Application Number : 750794
Regulatory Info : OTC
Registration Country : Canada
Regulatory Info : Generic
Registration Country : India
Brand Name :
Dosage Form : Eye Drop
Dosage Strength : 0.0255% W/V
Packaging : 5ml
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : India
Regulatory Info : Generic
Registration Country : South Korea
Pheniramine; Naphazoline Hydrochloride
Brand Name : NAZOLIN
Dosage Form : EYE DROP
Dosage Strength : 3MG/ML; 0.25MG/ML
Packaging : 15mL
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Korea
Regulatory Info : Generic
Registration Country : South Korea
Aminocaproic Acid; Neostigmine Methyl Sulfate; Naphazoline Hydrochloride; Chlorpheniramine Maleate
Brand Name : EYEFEEL
Dosage Form : EYE DROP
Dosage Strength : 10MG/ML; 0.02MG/ML; 0.02MG/ML; 0.1MG/ML
Packaging : 15mL
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Korea
Regulatory Info : Generic
Registration Country : South Korea
Naphazoline Hydrochloride; Glycerol
Brand Name : MAXIMUM REDNESS RELIEF
Dosage Form : EYE DROP
Dosage Strength : 0.3MG/ML; 5MG/ML
Packaging : 15mL
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Korea
Regulatory Info : Generic
Registration Country : South Korea
Glycerol; Naphazoline Hydrochloride
Brand Name : REDNESS RELIEF
Dosage Form : EYE DROP
Dosage Strength : 2.5MG/ML; 0.12MG/ML
Packaging : 15mL
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Korea
Regulatory Info : OTC
Registration Country : USA
NAPHAZOLINE HYDROCHLORIDE; PHENIRAMINE MALEATE
Brand Name : VISINE
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : 0.025%;0.3%
Packaging :
Approval Date : 1996-01-31
Application Number : 20485
Regulatory Info : OTC
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
ANTAZOLINE PHOSPHATE; NAPHAZOLINE HYDROCHLORIDE
Brand Name : VASOCON-A
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : 0.5%;0.05%
Packaging :
Approval Date : 1994-07-11
Application Number : 18746
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : VASOCON
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : 0.1%
Packaging :
Approval Date : 1983-03-24
Application Number : 80235
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info :
Registration Country : Iran
Brand Name :
Dosage Form : Ophthalmic Drop
Dosage Strength : 0.1%
Packaging : 10 ML
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Iran
Regulatory Info :
Registration Country : Iran
Brand Name :
Dosage Form : Nasal Spray
Dosage Strength : 0.05%
Packaging : 15 ML
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Iran
Regulatory Info : DISCN
Registration Country : USA
Brand Name : NAPHAZOLINE HYDROCHLORIDE
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : 0.1%
Packaging :
Approval Date : 1982-01-01
Application Number : 83590
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : OTC
Registration Country : USA
NAPHAZOLINE HYDROCHLORIDE; PHENIRAMINE MALEATE
Brand Name : NAPHAZOLINE HYDROCHLORIDE AND PHENIRAMINE MALEATE
Dosage Form : SOLUTION/DROPS;OPHTHALMIC
Dosage Strength : 0.025%;0.3%
Packaging :
Approval Date : 2013-01-24
Application Number : 202795
Regulatory Info : OTC
Registration Country : USA
Regulatory Info : Generic
Registration Country : Turkey
Naphazoline Hydrochloride; Chlorpheniramine Maleate
Brand Name :
Dosage Form : NASAL SPRAY
Dosage Strength : 0.5MG; 5MG
Packaging : 15 Ml/Bottle
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : Turkey
Regulatory Info : Generic
Registration Country : Turkey
Naphazoline Hydrochloride; Chlorpheniramine Maleate
Brand Name :
Dosage Form : EYE AND NOSE DROPS
Dosage Strength : 0.05%; 0.05%
Packaging : 15 Ml/Bottle
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : Turkey
Regulatory Info : Generic
Registration Country : Turkey
Sulfacetamide; Zinc; Naphazoline Hydrochloride; Lidocaine
Brand Name :
Dosage Form : EYE DROPS
Dosage Strength : 30MG; 5MG; 0.05MG; 7MG
Packaging : 10 Ml/Bottle
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : Turkey
Regulatory Info :
Registration Country : Sweden
Brand Name : Cleari
Dosage Form : EYE DROPS, SOLUTION
Dosage Strength : 0.12 MG / ML
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
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