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 25DEXTROMETHORPHAN HYDROBROMIDE
15 2DICLOFENAC 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 4METHOCARBAMOL
34 10NICOTINE POLACRILEX
35 1NIZATIDINE
36 1ORLISTAT
37 1PERMETHRIN
38 3PHENIRAMINE MALEATE
39 9PHENYLEPHRINE HYDROCHLORIDE
40 15PSEUDOEPHEDRINE HYDROCHLORIDE
41 4Pantoprazole
42 3Paracetamol
43 3SIMETHICONE
44 1SULFUR
45 3XYLOMETAZOLINE HYDROCHLORIDE
46 1nicotine
47 1paracetamol
01 2HALEON AUSTRALIA PTY LTD
02 127HALEON 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 4GEL
07 1GEL;TOPICAL
08 6GUM, CHEWING;BUCCAL
09 4Gastro-Resistant Tablets
10 15KIT
11 1L?s
12 27POWDER 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 17TABLET
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04 10.05MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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09 11.34MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
10 110%
11 21000MG/SACHET
12 4100MG
13 1100MG/2.5ML
14 6100MG/5ML
15 1100MG/5ML;15MG/5ML
16 210MG
17 310MG/5ML
18 710MG/SACHET
19 112.5MG/20ML
20 112.5MG/5ML
21 2125MG
22 815MG
23 115MG/15ML
24 615MG/5ML
25 1180MG
26 11MG/5ML;100MG/5ML;15MG/5ML
27 11mg/ml
28 22.32%/W/W
29 220 mg
30 3200MG
31 4200MG/5ML
32 1200MG;10MG
33 1200MG;30MG
34 120MG/20ML
35 220MG/5ML
36 420MG/SACHET
37 121 mg/24 hours
38 122MG/5ML
39 3250MG
40 1250MG;125MG
41 1250MG;250MG;65MG
42 125MG
43 225MG/SACHET
44 125MG;EQ 200MG FREE ACID AND POTASSIUM SALT
45 12MG
46 12MG/15ML
47 12MG/5ML
48 12MG;200MG;30MG
49 13.125MG/5ML
50 930MG
51 130MG/15ML
52 130MG/20ML
53 130MG/5ML
54 230MG/SACHET
55 7325MG
56 2325MG/5ML
57 1325MG/SACHET
58 133.32%
59 138MG;200MG
60 240 mg
61 3400MG
62 1400MG/20ML
63 14MG/SACHET
64 24MG;200MG;10MG
65 15%/W/W
66 150%/W/W
67 2500 mg
68 3500MG
69 1500MG/15ML
70 1500MG/SACHET
71 150MCG/ACT
72 150MG
73 150MG/1.25ML
74 150MG/5ML
75 25MG/5ML
76 36.25MG
77 160MG
78 260MG/SACHET
79 5650MG/SACHET
80 37.5MG/5ML
81 2750MG
82 175MG
83 180MG
84 18MG
85 1EQ 200MG BASE
86 2EQ 200MG FREE ACID AND POTASSIUM SALT
87 1EQ 200MG FREE ACID AND POTASSIUM SALT;30MG
88 5EQ 2MG BASE
89 5EQ 4MG BASE
90 2Blank
01 2Australia
02 127Canada
03 4Italy
04 3Norway
05 3Switzerland
06 43USA
Regulatory Info :
Registration Country : Canada
Dosage Form : POWDER FOR SOLUTION
Brand Name : NEOCITRAN ULTRA STRENGTH ...
Dosage Strength : 1000MG/SACHET
Packaging : 10
Approval Date :
Application Number : 2217147
Regulatory Info :
Registration Country : Canada
Regulatory Info :
Registration Country : Canada
Dosage Form : POWDER FOR SOLUTION
Brand Name : NEOCITRAN EXTRA STRENGTH ...
Dosage Strength : 650MG/SACHET
Packaging : 10
Approval Date :
Application Number : 2293994
Regulatory Info :
Registration Country : Canada
Regulatory Info :
Registration Country : Canada
Dosage Form : TABLET
Brand Name : ROBAXACET
Dosage Strength : 325MG
Packaging : 18/40
Approval Date :
Application Number : 2026805
Regulatory Info :
Registration Country : Canada
Regulatory Info :
Registration Country : Canada
Dosage Form : POWDER FOR SOLUTION
Brand Name : NEOCITRAN EXTRA STRENGTH ...
Dosage Strength : 650MG/SACHET
Packaging : 10 POUCHES
Approval Date :
Application Number : 843792
Regulatory Info :
Registration Country : Canada
Regulatory Info :
Registration Country : Canada
Dosage Form : TABLET
Brand Name : ROBAXACET-8
Dosage Strength : 325MG
Packaging :
Approval Date :
Application Number : 1934767
Regulatory Info :
Registration Country : Canada
Regulatory Info :
Registration Country : Canada
Dosage Form : SOLUTION
Brand Name : BUCKLEY'S COMPLETE
Dosage Strength : 325MG/5ML
Packaging :
Approval Date :
Application Number : 2279703
Regulatory Info :
Registration Country : Canada
Regulatory Info :
Registration Country : Canada
Dosage Form : KIT
Brand Name : BUCKLEY'S COLD & SINUS 24...
Dosage Strength : 325MG
Packaging :
Approval Date :
Application Number : 2493802
Regulatory Info :
Registration Country : Canada
Regulatory Info :
Registration Country : Canada
Dosage Form : KIT
Brand Name : BUCKLEY'S COMPLETE 24 HOU...
Dosage Strength : 325MG
Packaging :
Approval Date :
Application Number : 2494027
Regulatory Info :
Registration Country : Canada
Regulatory Info :
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 :
Registration Country : Canada
Regulatory Info :
Registration Country : Canada
Dosage Form : CAPSULE
Brand Name : BUCKLEY'S COMPLETE + MUCU...
Dosage Strength : 250MG
Packaging :
Approval Date :
Application Number : 2335948
Regulatory Info :
Registration Country : Canada
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