MedPath

Hydrocortisone Acetate/Pramoxine Hydrochloride

Generic Name
Hydrocortisone Acetate/Pramoxine Hydrochloride

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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