Overview
Padimate O is an active sunscreen agent in cosmetics and over-the-counter sunscreen drug products in concentrations up to 8%, as regulated by the FDA . It is a structurally-related compound to Aminobenzoic acid that absorbs UV-B rays to prevent photodamage. It penetrates human skin, and is shown to induce non-ligatable strand breaks on DNA in vitro and mutagenic effects on yeast in vivo .
Indication
Indicated as an active UV-B filter to prevent photodamage.
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 |
|---|---|---|---|---|---|
| No FDA approvals found for this drug. | |||||
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 |
|---|---|---|---|---|---|
| JOHN PLUNKETT'S SUPERFADE SKIN CREAM tube | 341504 | Medicine | A | 8/13/2020 | |
| BLISTEX MEDICATED RELIEF ointment tube | 14883 | Medicine | A | 9/5/1991 | |
| JOHN PLUNKETT’S SUPERFADE FACE TREATMENT CREAM tube | 11629 | Medicine | A | 9/12/1991 | |
| Superfade Cream | 197217 | Medicine | A | 5/4/2012 | |
| JOHN PLUNKETT'S SUPERFADE TREATMENT CREAM tube | 52376 | Medicine | A | 5/25/1995 |
Health Canada Drug Approvals
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
|---|---|---|---|---|---|
| GROOMING GEAR AFTER SHAVE TREATMENT LOT 2.5% | amway corporation | 02065827 | Lotion - Topical | 2.5 % | 12/31/1994 |
| ZARINA SKIN LIGHTENING CREAM WITH SUNSCREENING FILTER | fairtrade international co. ltd. | 02266490 | Cream - Topical | 4.5 % | N/A |
| ESOTERICA SCENTED-FORTIFIED WITH SUNSCREEN | 02029944 | Cream - Topical | 3.3 % | 12/31/1960 | |
| LOTION SOLAIRE - 15 | rolmex international inc. | 02010518 | Lotion - Topical | 7 MG / 100 MG | 12/31/1994 |
| CAP SOLEIL: LAIT SOLAIRE FPS 4 | yves rocher inc. | 02221179 | Lotion - Topical | 2.5 % | 10/26/1998 |
| BANANA BOAT DARK TANNING OIL SPF 8 | the banana boat company | 02240767 | Liquid - Topical | 4.5 % | 2/17/2000 |
| HYDRA ADVANCE SOLAIRE LAIT SPF 15 | yves rocher inc. | 02182319 | Emulsion - Topical | 7 % | 12/31/1995 |
| DERMATONE LIP BALM | dermatone laboratories, inc. | 02097451 | Ointment - Topical | 7 % | 12/31/1989 |
| SHAKLEE LIP PROTECTION STICK SPF 15 | shaklee canada inc | 00670723 | Stick - Topical | 6 % | 12/31/1986 |
| SUN LIPCARE SPF 18 | avalon natural products | 02245364 | Stick - Topical | 6 % | 2/1/2003 |
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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