Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
01 2Sanofi
02 2CeraVe
03 2Church & Dwight Co
04 2DERMTEK PHARMA INC
05 1Ferndale Laboratories, Inc.
06 1Genus Lifesciences
07 4Johnson & Johnson
08 1Kolmar Korea Co., Ltd.
09 4Legacy Pharma
10 2ODAN LABORATORIES LTD
11 2Pharmascience Inc.
12 1T.M.Thakore Pharmaceutical Laboratories
13 2Viatris
01 3AEROSOL, METERED;TOPICAL
02 3CREAM
03 2CREAM;TOPICAL
04 2Cream
05 5LOTION
06 3LOTION;TOPICAL
07 1OIN
08 4OINTMENT
09 1SUP
10 2SUPPOSITORY
01 2DISCN
02 12OTC
03 2Originator
04 2Prescription
05 6RX
06 2Blank
01 1ANUSOL PLUS OINTMENT
02 1ANUSOL PLUS SUPPOSITORIES
03 1AVEENO ANTI-ITCH LOTION
04 1Antibiotic Cream
05 1Anugesic
06 1Anusol Pain Relief Ointment
07 1EPIFOAM
08 1GOLD BOND ANTI-ITCH LOTION
09 1GOLD BOND MEDICATED ANTI-ITCH CREAM
10 2HEMORRHOIDAL OINTMENT
11 1HYDROCORTISONE ACETATE 1% AND PRAMOXINE HYDROCHLORIDE 1%
12 1ITCH RELIEF MOISTURIZING CREAM
13 1ITCH RELIEF MOISTURIZING LOTION
14 1POLYSPORIN ITCH RELIEF
15 5PRAMOSONE
16 1PRAMOX HC CREAM
17 1PRAMOX HC LOTION
18 1PROCTODAN-HC OINTMENT
19 1PROCTODAN-HC SUPPOSITORIES
20 1PROCTOFOAM HC
21 1Blank
01 14Canada
02 1India
03 2South Africa
04 1South Korea
05 8USA
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info : OTC
Registration Country : Canada
Brand Name : GOLD BOND MEDICATED ANTI-ITCH CREAM
Dosage Form : CREAM
Dosage Strength : 1%/W/W
Packaging : 28G
Approval Date :
Application Number : 2236991
Regulatory Info : OTC
Registration Country : Canada
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info : OTC
Registration Country : Canada
Brand Name : GOLD BOND ANTI-ITCH LOTION
Dosage Form : LOTION
Dosage Strength : 1%/W/W
Packaging : 155ML
Approval Date :
Application Number : 2318482
Regulatory Info : OTC
Registration Country : Canada
Regulatory Info : OTC
Registration Country : Canada
Brand Name : ITCH RELIEF MOISTURIZING CREAM
Dosage Form : CREAM
Dosage Strength : 1%/W/W
Packaging :
Approval Date :
Application Number : 2484889
Regulatory Info : OTC
Registration Country : Canada
Regulatory Info : OTC
Registration Country : Canada
Brand Name : ITCH RELIEF MOISTURIZING LOTION
Dosage Form : LOTION
Dosage Strength : 1%
Packaging :
Approval Date :
Application Number : 2486881
Regulatory Info : OTC
Registration Country : Canada
Regulatory Info : OTC
Registration Country : Canada
Brand Name : ANUSOL PLUS OINTMENT
Dosage Form : OINTMENT
Dosage Strength : 1%
Packaging : 30G
Approval Date :
Application Number : 1945912
Regulatory Info : OTC
Registration Country : Canada
Regulatory Info : OTC
Registration Country : Canada
Brand Name : ANUSOL PLUS SUPPOSITORIES
Dosage Form : SUPPOSITORY
Dosage Strength : 20MG
Packaging : Dec-24
Approval Date :
Application Number : 1945904
Regulatory Info : OTC
Registration Country : Canada
Regulatory Info : OTC
Registration Country : Canada
Brand Name : PRAMOX HC CREAM
Dosage Form : CREAM
Dosage Strength : 1%
Packaging : 45GM
Approval Date :
Application Number : 770957
Regulatory Info : OTC
Registration Country : Canada
Regulatory Info : OTC
Registration Country : Canada
Brand Name : PRAMOX HC LOTION
Dosage Form : LOTION
Dosage Strength : 1%
Packaging : 120ML
Approval Date :
Application Number : 1954210
Regulatory Info : OTC
Registration Country : Canada
Regulatory Info : DISCN
Registration Country : USA
HYDROCORTISONE ACETATE; PRAMOXINE HYDROCHLORIDE
Brand Name : PRAMOSONE
Dosage Form : LOTION;TOPICAL
Dosage Strength : 0.5%;1%
Packaging :
Approval Date : 1982-01-01
Application Number : 83213
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
HYDROCORTISONE ACETATE; PRAMOXINE HYDROCHLORIDE
Brand Name : HYDROCORTISONE ACETATE 1% AND PRAMOXINE HYDROCHLORIDE 1%
Dosage Form : AEROSOL, METERED;TOPICAL
Dosage Strength : 1%;1%
Packaging :
Approval Date : 1988-05-17
Application Number : 89440
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : OTC
Registration Country : Canada
Brand Name : AVEENO ANTI-ITCH LOTION
Dosage Form : LOTION
Dosage Strength : 1%
Packaging : 118ML
Approval Date :
Application Number : 2240105
Regulatory Info : OTC
Registration Country : Canada
Regulatory Info : OTC
Registration Country : Canada
Brand Name : POLYSPORIN ITCH RELIEF
Dosage Form : LOTION
Dosage Strength : 1%
Packaging : 177ML
Approval Date :
Application Number : 2246156
Regulatory Info : OTC
Registration Country : Canada
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : Anugesic
Dosage Form : SUP
Dosage Strength : 140ug/cm²
Packaging : 10X1mg/supp
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : Anusol Pain Relief Ointment
Dosage Form : OIN
Dosage Strength : 10mg/g
Packaging : 25X1mg/g
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info :
Registration Country : South Korea
Neomycin Sulfate; POLYMYXIN B SULFATE; Pramoxine
Brand Name : Antibiotic Cream
Dosage Form : Cream
Dosage Strength : 3.5MG; 10000Units; 10MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : South Korea
Regulatory Info : RX
Registration Country : USA
HYDROCORTISONE ACETATE; PRAMOXINE HYDROCHLORIDE
Brand Name : PRAMOSONE
Dosage Form : CREAM;TOPICAL
Dosage Strength : 0.5%;1%
Packaging :
Approval Date : 1982-01-01
Application Number : 83778
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
HYDROCORTISONE ACETATE; PRAMOXINE HYDROCHLORIDE
Brand Name : PRAMOSONE
Dosage Form : CREAM;TOPICAL
Dosage Strength : 1%;1%
Packaging :
Approval Date : 1982-01-01
Application Number : 85368
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
HYDROCORTISONE ACETATE; PRAMOXINE HYDROCHLORIDE
Brand Name : PRAMOSONE
Dosage Form : LOTION;TOPICAL
Dosage Strength : 2.5%;1%
Packaging :
Approval Date : 1982-01-01
Application Number : 85979
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
HYDROCORTISONE ACETATE; PRAMOXINE HYDROCHLORIDE
Brand Name : PRAMOSONE
Dosage Form : LOTION;TOPICAL
Dosage Strength : 1%;1%
Packaging :
Approval Date : 1982-01-01
Application Number : 85980
Regulatory Info : RX
Registration Country : USA
Regulatory Info : Prescription
Registration Country : Canada
Brand Name : PROCTODAN-HC OINTMENT
Dosage Form : OINTMENT
Dosage Strength : 1%
Packaging : 15G/30G
Approval Date :
Application Number : 2234466
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
Brand Name : PROCTODAN-HC SUPPOSITORIES
Dosage Form : SUPPOSITORY
Dosage Strength : 20MG
Packaging : 12
Approval Date :
Application Number : 2240851
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : OTC
Registration Country : Canada
Brand Name : HEMORRHOIDAL OINTMENT
Dosage Form : OINTMENT
Dosage Strength : 0.01MG
Packaging : 30G
Approval Date :
Application Number :
Regulatory Info : OTC
Registration Country : Canada
Regulatory Info : OTC
Registration Country : Canada
Brand Name : HEMORRHOIDAL OINTMENT
Dosage Form : OINTMENT
Dosage Strength : 0.01MG
Packaging : 30G
Approval Date :
Application Number :
Regulatory Info : OTC
Registration Country : Canada
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Cream
Dosage Strength : 1%
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info : RX
Registration Country : USA
HYDROCORTISONE ACETATE; PRAMOXINE HYDROCHLORIDE
Brand Name : PROCTOFOAM HC
Dosage Form : AEROSOL, METERED;TOPICAL
Dosage Strength : 1%;1%
Packaging :
Approval Date : 1982-01-01
Application Number : 86195
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
HYDROCORTISONE ACETATE; PRAMOXINE HYDROCHLORIDE
Brand Name : EPIFOAM
Dosage Form : AEROSOL, METERED;TOPICAL
Dosage Strength : 1%;1%
Packaging :
Approval Date : 1982-01-01
Application Number : 86457
Regulatory Info : RX
Registration Country : USA
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