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DERMA WHITE
DERMA WHITE - 49527-008-01 - (OCTINOXATE, TITANIUM DIOXIDE, OCTISALATE)
Drug Information of DERMA WHITE
| Product NDC: | 49527-008 |
| Proprietary Name: | DERMA WHITE |
| Non Proprietary Name: | OCTINOXATE, TITANIUM DIOXIDE, OCTISALATE |
| Active Ingredient(s): | 7.5; 2; 5.2 mL/100mL; mL/100mL; mL/100mL & nbsp; OCTINOXATE, TITANIUM DIOXIDE, OCTISALATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DERMA WHITE
| Product NDC: | 49527-008 |
| Labeler Name: | CLINIQUE LABS INC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20101001 |
Package Information of DERMA WHITE
| Package NDC: | 49527-008-01 |
| Package Description: | 1 TUBE in 1 CARTON (49527-008-01) > 30 mL in 1 TUBE (49527-008-02) |
NDC Information of DERMA WHITE
| NDC Code | 49527-008-01 |
| Proprietary Name | DERMA WHITE |
| Package Description | 1 TUBE in 1 CARTON (49527-008-01) > 30 mL in 1 TUBE (49527-008-02) |
| Product NDC | 49527-008 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, TITANIUM DIOXIDE, OCTISALATE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20101001 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | CLINIQUE LABS INC |
| Substance Name | OCTINOXATE; OCTISALATE; TITANIUM DIOXIDE |
| Strength Number | 7.5; 2; 5.2 |
| Strength Unit | mL/100mL; mL/100mL; mL/100mL |
| Pharmaceutical Classes |
