01 24ACETAMINOPHEN
02 1ACETAMINOPHEN; ASPIRIN; CAFFEINE
03 1ACETAMINOPHEN; IBUPROFEN
04 1ACETYLSALICYLIC ACID
05 1BROMPHENIRAMINE MALEATE
06 1Benzododecinium Bromide; Sodium Chloride; Polysorbate 80
07 1CALCIUM CARBONATE
08 3CHLORPHENIRAMINE MALEATE
09 2CHLORPHENIRAMINE MALEATE; IBUPROFEN; PHENYLEPHRINE HYDROCHLORIDE
10 2CHLORPHENIRAMINE MALEATE; IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE
11 1CLEMASTINE FUMARATE
12 1CLOBETASONE BUTYRATE
13 1CODEINE PHOSPHATE
14 24DEXTROMETHORPHAN HYDROBROMIDE
15 4DICLOFENAC DIETHYLAMINE
16 1DICLOFENAC SODIUM
17 1DIPHENHYDRAMINE CITRATE; IBUPROFEN
18 4DIPHENHYDRAMINE HYDROCHLORIDE
19 1DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN
20 1DOCOSANOL
21 5DOXYLAMINE SUCCINATE
22 1Diclofenac sodium
23 1Dimetindeni maleas
24 1FLUTICASONE FUROATE
25 3FLUTICASONE PROPIONATE
26 11GUAIFENESIN
27 1HAMAMELIS VIRGINIANA
28 14IBUPROFEN
29 1IBUPROFEN SODIUM
30 1IBUPROFEN; PHENYLEPHRINE HYDROCHLORIDE
31 3IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE
32 5MENTHOL
33 5METHOCARBAMOL
34 10NICOTINE POLACRILEX
35 1NIZATIDINE
36 1Nicotine
37 1ORLISTAT
38 1PERMETHRIN
39 3PHENIRAMINE MALEATE
40 8PHENYLEPHRINE HYDROCHLORIDE
41 15PSEUDOEPHEDRINE HYDROCHLORIDE
42 4Pantoprazole
43 4Paracetamol
44 3SIMETHICONE
45 1SULFUR
46 3XYLOMETAZOLINE HYDROCHLORIDE
01 2HALEON AUSTRALIA PTY LTD
02 128HALEON CANADA ULC
03 4HALEON ITALY SRL
04 42HALEON US HOLDINGS
05 3Haleon Denmark ApS
06 3Haleon Schweiz AG
07 1POYTHRESS
01 16CAPSULE
02 5CAPSULE;ORAL
03 2CREAM
04 1CREAM;TOPICAL
05 1Emulgel
06 6GEL
07 1GEL;TOPICAL
08 6GUM, CHEWING;BUCCAL
09 4Gastro-Resistant Tablets
10 15KIT
11 1L?s
12 24POWDER FOR SOLUTION
13 1POWDER;TOPICAL
14 3SOLUTION
15 3SPRAY
16 1SPRAY, METERED DOSE
17 3SPRAY, METERED;NASAL
18 2SUSPENSION/DROPS;ORAL
19 5SUSPENSION;ORAL
20 36SYRUP
21 19TABLET
22 3TABLET (CHEWABLE)
23 2TABLET, CHEWABLE;ORAL
24 13TABLET;ORAL
25 4TROCHE/LOZENGE;ORAL
26 3Tablet, film-coated
27 1Tropfen
28 2Blank
01 10.0275MG/SPRAY
02 10.05%/W/W
03 10.05MG/SPRAY
04 10.05MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
05 30.1%/W/V
06 10.25%/W/W
07 11 g
08 21%
09 21.16%/W/W
10 11.34MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
11 110%
12 21000MG/SACHET
13 4100MG
14 1100MG/2.5ML
15 6100MG/5ML
16 1100MG/5ML;15MG/5ML
17 210MG
18 310MG/5ML
19 610MG/SACHET
20 112.5MG/20ML
21 112.5MG/5ML
22 2125MG
23 815MG
24 115MG/15ML
25 615MG/5ML
26 1180MG
27 11MG/5ML;100MG/5ML;15MG/5ML
28 11mg/ml
29 22.32%/W/W
30 220 mg
31 3200MG
32 4200MG/5ML
33 1200MG;10MG
34 1200MG;30MG
35 120MG/20ML
36 220MG/5ML
37 320MG/SACHET
38 121 mg/24 hours
39 122MG/5ML
40 3250MG
41 1250MG;125MG
42 1250MG;250MG;65MG
43 125MG
44 225MG/SACHET
45 125MG;EQ 200MG FREE ACID AND POTASSIUM SALT
46 12MG
47 12MG/15ML
48 12MG/5ML
49 12MG;200MG;30MG
50 13.125MG/5ML
51 930MG
52 130MG/15ML
53 130MG/20ML
54 130MG/5ML
55 230MG/SACHET
56 7325MG
57 2325MG/5ML
58 1325MG/SACHET
59 133.32%
60 138MG;200MG
61 240 mg
62 4400MG
63 1400MG/20ML
64 14MG/SACHET
65 24MG;200MG;10MG
66 15%/W/W
67 150%/W/W
68 2500 mg
69 4500MG
70 1500MG/15ML
71 1500MG/SACHET
72 150MCG/ACT
73 150MG
74 150MG/1.25ML
75 150MG/5ML
76 25MG/5ML
77 36.25MG
78 160MG
79 260MG/SACHET
80 4650MG/SACHET
81 37.5MG/5ML
82 2750MG
83 175MG
84 180MG
85 18MG
86 1EQ 200MG BASE
87 2EQ 200MG FREE ACID AND POTASSIUM SALT
88 1EQ 200MG FREE ACID AND POTASSIUM SALT;30MG
89 5EQ 2MG BASE
90 5EQ 4MG BASE
91 2Blank
01 2Australia
02 128Canada
03 4Italy
04 3Norway
05 3Switzerland
06 43USA
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 : 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 : 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 : 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 : 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 : 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
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 : 2409178
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 :
Approval Date :
Application Number : 2215403
Regulatory Info : OTC
Registration Country : Canada
