Overview
No overview information available.
Indication
No indication information available.
Associated Conditions
No associated conditions information available.
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
---|
No clinical trials found
No clinical trials found for this drug
FDA Drug Approvals
Approved Product | Manufacturer | NDC Code | Route | Strength | Effective Date |
---|---|---|---|---|---|
Trifecta Pharmaceuticals USA | 69396-061 | TOPICAL | 10 mg in 100 g | 5/12/2025 | |
Padagis Israel Pharmaceuticals Ltd | 45802-144 | TOPICAL | 1 g in 100 g | 3/15/2018 | |
Bryant Ranch Prepack | 63629-8672 | TOPICAL | 1 g in 100 g | 7/18/2023 | |
Click Industries LLC | 86173-886 | TOPICAL | 0.5 g in 100 mL | 3/11/2025 | |
Sebela Pharmaceuticals Inc. | 54766-829 | TOPICAL | 10 mg in 1 mL | 12/15/2017 | |
Pageview Pharmaceuticals | 73028-401 | RECTAL | 18 mg in 1 1 | 2/1/2022 | |
Womens Choice Pharmaceuticals LLC | 50967-357 | TOPICAL | 11.5 mg in 1 g | 1/18/2023 | |
Strategic Sourcing Services LLC | 62011-0099 | TOPICAL | 10 mg in 1 g | 7/7/2025 | |
Sebela Pharmaceuticals Inc. | 54766-763 | TOPICAL | 10 mg in 1 g | 12/15/2017 | |
Rebel Distributors Corp | 21695-982 | TOPICAL | 100 mg in 10 g | 11/5/2010 |
EMA Drug Approvals
Approved Product | Authorization Holder | Status | Issued Date |
---|---|---|---|
No EMA approvals found for this drug. |
HSA Drug Approvals
Approved Product | Manufacturer | Approval Number | Dosage Form | Strength | Approval Date |
---|---|---|---|---|---|
No HSA approvals found for this drug. |
NMPA Drug Approvals
Approved Product | Company | Approval Number | Drug Type | Dosage Form | Approval Date |
---|---|---|---|---|---|
No NMPA approvals found for this drug. |
PPB Drug Approvals
Approved Product | Registration No. | Company | Licence No. | Strength | Registration Date |
---|---|---|---|---|---|
No PPB approvals found for this drug. |
TGA Drug Approvals
Approved Product | ARTG ID | Sponsor | Registration Type | Status | Registration Date |
---|---|---|---|---|---|
No TGA approvals found for this drug. |
Health Canada Drug Approvals
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
---|---|---|---|---|---|
GOLD BOND MEDICATED ANTI-ITCH CREAM | sanofi consumer health inc | 02236991 | Cream - Topical | 1 % / W/W | 1/11/1999 |
HEMORRHOIDAL OINTMENT WITH ANESTHETIC FOR EXTRA PAIN RELIEF | cellchem pharmaceuticals inc. | 02295865 | Ointment - Rectal | 1 % / W/W | N/A |
CLEAR ANTI-ITCH LOTION | lander co. canada limited | 02244180 | Lotion - Topical | 1.0 % | 10/2/2001 |
BIKINI ZONE MEDICATED AFTER SHAVE SPRAY | cca industries, inc. | 02420074 | Liquid - Topical | 1 % | N/A |
HEMORRHOIDAL OINTMENT | 02218887 | Ointment - Rectal | 1.0 % / W/W | 3/17/1997 | |
W15883-CS | warner-lambert canada inc. | 02240584 | Ointment - Topical | 1 % | N/A |
ITCH RELIEF BALM | johnson & johnson inc | 02486385 | Ointment - Topical | 0.5 % / W/W | 7/20/2020 |
CLEAR ANTI-ITCH LOTION | perrigo international | 02230493 | Lotion - Topical | 1 % | 8/17/1998 |
ANUSOL PLUS OINTMENT | church & dwight canada corp | 01945912 | Ointment - Rectal
,
Topical | 1 % | 12/31/1992 |
ITCH RELIEF LOTION | crls | 02318423 | Lotion - Topical | 1.0 % / W/W | 9/9/2009 |
CIMA AEMPS Drug Approvals
Approved Product | Company | Registration Number | Pharmaceutical Form | Prescription Type | Status |
---|---|---|---|---|---|
No CIMA AEMPS (Spain) approvals found for this drug. |
Philippines FDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
---|---|---|---|---|---|
No Philippines FDA approvals found for this drug. |
Saudi SFDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
---|---|---|---|---|---|
No Saudi SFDA approvals found for this drug. |
Malaysia NPRA Drug Approvals
Approved Product | Company | Registration Number | Dosage Form | Strength | Approval Date |
---|---|---|---|---|---|
No Malaysia NPRA approvals found for this drug. |
UK EMC Drug Information
Medicine Name | MA Holder | MA Number | Pharmaceutical Form | Active Ingredient | Authorization Date |
---|---|---|---|---|---|
No UK EMC drug information found for this drug. |
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