01 22ACETAMINOPHEN
02 1ACETAMINOPHEN; ASPIRIN; CAFFEINE
03 1ACETAMINOPHEN; IBUPROFEN
04 1BROMPHENIRAMINE MALEATE
05 1Benzododecinium Bromide; Sodium Chloride; Polysorbate 80
06 1CALCIUM CARBONATE
07 3CHLORPHENIRAMINE MALEATE
08 2CHLORPHENIRAMINE MALEATE; IBUPROFEN; PHENYLEPHRINE HYDROCHLORIDE
09 2CHLORPHENIRAMINE MALEATE; IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE
10 1CLEMASTINE FUMARATE
11 22DEXTROMETHORPHAN HYDROBROMIDE
12 1DICLOFENAC SODIUM
13 1DIPHENHYDRAMINE CITRATE; IBUPROFEN
14 3DIPHENHYDRAMINE HYDROCHLORIDE
15 1DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN
16 1DOCOSANOL
17 4DOXYLAMINE SUCCINATE
18 1Diclofenac sodium
19 1Dimetindeni maleas
20 1FLUTICASONE FUROATE
21 3FLUTICASONE PROPIONATE
22 10GUAIFENESIN
23 12IBUPROFEN
24 1IBUPROFEN SODIUM
25 1IBUPROFEN; PHENYLEPHRINE HYDROCHLORIDE
26 3IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE
27 5MENTHOL
28 10NICOTINE POLACRILEX
29 1NIZATIDINE
30 1ORLISTAT
31 1PERMETHRIN
32 3PHENIRAMINE MALEATE
33 8PHENYLEPHRINE HYDROCHLORIDE
34 14PSEUDOEPHEDRINE HYDROCHLORIDE
35 4Pantoprazole
36 3Paracetamol
37 3SIMETHICONE
38 1SULFUR
39 3XYLOMETAZOLINE HYDROCHLORIDE
40 1nicotine
41 1paracetamol
01 2HALEON AUSTRALIA PTY LTD
02 105HALEON CANADA ULC
03 4HALEON ITALY SRL
04 42HALEON US HOLDINGS
05 3Haleon Denmark ApS
06 3Haleon Schweiz AG
07 1POYTHRESS
01 13CAPSULE
02 5CAPSULE;ORAL
03 1CREAM
04 1CREAM;TOPICAL
05 1Emulgel
06 1GEL;TOPICAL
07 6GUM, CHEWING;BUCCAL
08 4Gastro-Resistant Tablets
09 15KIT
10 1L?s
11 27POWDER FOR SOLUTION
12 1POWDER;TOPICAL
13 3SOLUTION
14 3SPRAY
15 1SPRAY, METERED DOSE
16 3SPRAY, METERED;NASAL
17 2SUSPENSION/DROPS;ORAL
18 5SUSPENSION;ORAL
19 30SYRUP
20 9TABLET
21 3TABLET (CHEWABLE)
22 2TABLET, CHEWABLE;ORAL
23 13TABLET;ORAL
24 4TROCHE/LOZENGE;ORAL
25 3Tablet, film-coated
26 1Tropfen
27 2Blank
01 10.0275MG/SPRAY
02 10.05MG/SPRAY
03 10.05MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
04 30.1%/W/V
05 11 g
06 21%
07 11.34MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
08 110%
09 21000MG/SACHET
10 4100MG
11 1100MG/2.5ML
12 6100MG/5ML
13 1100MG/5ML;15MG/5ML
14 210MG
15 310MG/5ML
16 710MG/SACHET
17 112.5MG/20ML
18 112.5MG/5ML
19 2125MG
20 815MG
21 115MG/15ML
22 515MG/5ML
23 1180MG
24 11MG/5ML;100MG/5ML;15MG/5ML
25 11mg/ml
26 220 mg
27 1200MG
28 4200MG/5ML
29 1200MG;10MG
30 1200MG;30MG
31 120MG/20ML
32 220MG/5ML
33 420MG/SACHET
34 121 mg/24 hours
35 122MG/5ML
36 3250MG
37 1250MG;125MG
38 1250MG;250MG;65MG
39 225MG/SACHET
40 125MG;EQ 200MG FREE ACID AND POTASSIUM SALT
41 12MG
42 12MG/15ML
43 12MG/5ML
44 12MG;200MG;30MG
45 930MG
46 130MG/15ML
47 130MG/20ML
48 130MG/5ML
49 230MG/SACHET
50 5325MG
51 2325MG/5ML
52 1325MG/SACHET
53 133.32%
54 138MG;200MG
55 240 mg
56 1400MG/20ML
57 14MG/SACHET
58 24MG;200MG;10MG
59 15%/W/W
60 2500 mg
61 2500MG
62 1500MG/15ML
63 1500MG/SACHET
64 150MCG/ACT
65 150MG
66 150MG/1.25ML
67 15MG/5ML
68 36.25MG
69 160MG
70 260MG/SACHET
71 5650MG/SACHET
72 17.5MG/5ML
73 1750MG
74 175MG
75 180MG
76 1EQ 200MG BASE
77 2EQ 200MG FREE ACID AND POTASSIUM SALT
78 1EQ 200MG FREE ACID AND POTASSIUM SALT;30MG
79 5EQ 2MG BASE
80 5EQ 4MG BASE
81 2Blank
01 2Australia
02 105Canada
03 4Italy
04 3Norway
05 3Switzerland
06 43USA
Regulatory Info : OTC
Registration Country : Canada
Dosage Form : TABLET
Brand Name : BUCKLEY'S COMPLETE EXTRA ...
Dosage Strength : 500MG
Packaging :
Approval Date :
Application Number : 2241592
Regulatory Info : OTC
Registration Country : Canada
Regulatory Info : OTC
Registration Country : Canada
Dosage Form : SOLUTION
Brand Name : BUCKLEY'S COMPLETE
Dosage Strength : 325MG/5ML
Packaging :
Approval Date :
Application Number : 2279703
Regulatory Info : OTC
Registration Country : Canada
Regulatory Info : OTC
Registration Country : Canada
Dosage Form : KIT
Brand Name : BUCKLEY'S COLD & SINUS 24...
Dosage Strength : 325MG
Packaging :
Approval Date :
Application Number : 2493802
Regulatory Info : OTC
Registration Country : Canada
Regulatory Info : OTC
Registration Country : Canada
Dosage Form : KIT
Brand Name : BUCKLEY'S COMPLETE 24 HOU...
Dosage Strength : 250MG
Packaging :
Approval Date :
Application Number : 2494027
Regulatory Info : OTC
Registration Country : Canada
Regulatory Info : OTC
Registration Country : Canada
Dosage Form : SYRUP
Brand Name : BUCKLEY'S COMPLETE PLUS E...
Dosage Strength : 325MG/5ML
Packaging :
Approval Date :
Application Number : 2357232
Regulatory Info : OTC
Registration Country : Canada
Regulatory Info : OTC
Registration Country : Canada
Dosage Form : POWDER FOR SOLUTION
Brand Name : NEOCITRAN TOTAL COLD NIGH...
Dosage Strength : 500MG/SACHET
Packaging : 10 POUCHES
Approval Date :
Application Number : 2413280
Regulatory Info : OTC
Registration Country : Canada
Regulatory Info : OTC
Registration Country : Canada
Dosage Form : CAPSULE
Brand Name : BUCKLEYS COLD & SINUS
Dosage Strength : 325MG
Packaging :
Approval Date :
Application Number : 2307111
Regulatory Info : OTC
Registration Country : Canada
Regulatory Info : OTC
Registration Country : Canada
Dosage Form : SYRUP
Brand Name : ROBITUSSIN TOTAL COUGH, C...
Dosage Strength : 500MG/15ML
Packaging : 240ML
Approval Date :
Application Number : 2291371
Regulatory Info : OTC
Registration Country : Canada
Regulatory Info : OTC
Registration Country : Canada
Dosage Form : CAPSULE
Brand Name : BUCKLEY'S COMPLETE + MUCU...
Dosage Strength : 250MG
Packaging :
Approval Date :
Application Number : 2335948
Regulatory Info : OTC
Registration Country : Canada
Regulatory Info : OTC
Registration Country : Canada
Dosage Form : POWDER FOR SOLUTION
Brand Name : NEOCITRAN EXTRA STRENGTH ...
Dosage Strength : 650MG/SACHET
Packaging : 10
Approval Date :
Application Number : 2456982
Regulatory Info : OTC
Registration Country : Canada
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